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SAHPRA Recalls Affected batches of Citro-Soda Regular Following Safety Concerns
LifestyleIn The News

SAHPRA Issues Urgent Recall on Citro-Soda Batches

by BabyYumYum March 27, 2026
written by BabyYumYum

Health and safety alerts can feel alarming, especially when they involve everyday products found in many homes. For families, knowing what to look out for is essential. Recent updates about the recall of affected batches of Citro-Soda Regular have raised important questions for consumers across South Africa. Staying informed and checking products carefully can help ensure your household remains safe while authorities work to address the issue.

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The South African Health Products Regulatory Authority (SAHPRA) has announced the recall of specific batches of Citro-Soda Regular products after identifying a potential safety risk. The move, communicated during a formal media briefing, reinforces SAHPRA’s ongoing commitment to safeguarding public health and ensuring that all health products in South Africa meet strict standards of quality, safety and efficacy.

Why Citro-Soda Regular Products Are Being Recalled

The recall follows a regulatory inspection at the Adcock Ingram manufacturing facility in Clayville, Johannesburg. During this inspection, SAHPRA identified a potential risk of foreign material contamination, prompting immediate precautionary action.

While no widespread harm has been confirmed, the regulator acted swiftly to minimise any possible risk to consumers. This type of recall forms part of SAHPRA’s risk-based oversight approach, which prioritises early intervention before issues escalate.

Affected Citro-Soda Products

The recall is limited to specific batches of the following Citro-Soda Regular products:

• Citro-Soda Regular 60 g
• Citro-Soda Regular 120 g
• Citro-Soda Regular 4 g x 30 Sachets

Consumers are advised to check batch numbers carefully against official recall notices. Only the identified batches are affected, and other Citro-Soda products remain available.

DOWNLOAD THE CITRO-SODA BATCH LIST HERE

What Consumers Should Do

SAHPRA has issued clear guidance for consumers who may have purchased the affected products:

• Stop using the product immediately if it falls within the recalled batches
• Return it to the nearest pharmacy, store or healthcare facility
• Seek medical advice if any unusual symptoms or side effects occur

Members of the public experiencing adverse reactions are urged to report these incidents directly to SAHPRA, helping strengthen ongoing monitoring and safety measures.

Retailers and Suppliers Given Immediate Instructions

Retail pharmacies, wholesalers and distribution centres across South Africa have been instructed to:

• Immediately stop selling the affected batches
• Remove all stock from shelves
• Return products to suppliers without delay

This coordinated response ensures that potentially compromised products are swiftly removed from circulation.

SAHPRA’s Commitment to Public Safety

Speaking during the briefing, SAHPRA CEO Dr Boitumelo Semete-Makokotlela emphasised the organisation’s unwavering focus on public well-being.

Speaking during the briefing, SAHPRA CEO Dr Boitumelo Semete-Makokotlela emphasised the organisation’s unwavering focus on public well-being

“The safety and well-being of the public remain our highest priority. SAHPRA will continue to act decisively and transparently to ensure that all health products on the market meet the required standards of quality, safety and efficacy,” she stated.

Ongoing Monitoring and Compliance

SAHPRA has confirmed that the recall process will be closely monitored to ensure all affected batches are fully removed and destroyed. In addition, the authority will continue to oversee compliance at the Clayville manufacturing facility until all required corrective and preventative actions have been implemented.

This includes:

• Continued inspections of the facility
• Verification of manufacturing processes
• Ensuring long-term compliance with regulatory standards

What This Means for South African Consumers

While recalls can raise concern, they are also a sign that regulatory systems are functioning effectively. SAHPRA’s proactive response demonstrates a commitment to transparency and accountability within South Africa’s healthcare system.

For consumers, the message is clear: remain vigilant, check product batches, and follow official guidance. For the broader industry, the recall serves as a reminder that quality control is non-negotiable, especially when public health is at stake.

As SAHPRA continues to monitor the situation, South Africans can be reassured that decisive steps are being taken to protect them — not after harm occurs, but before it has the chance to.

Source and Image: SAHPRA Official Press Release
https://www.sahpra.org.za/press-releases/sahpra-recalls-affected-batches-of-citro-soda-regular-following-safety-concerns/

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Clicks Recall: Toddler Snack Pulled From Shelves Over Listeria Contamination Concern Image credit: Instagram/clicksbaby_sa
ToddlersIn The NewsToddler Health

Clicks Recall: Toddler Snack Pulled From Shelves Over Listeria Contamination Concern

by Nokuthula Ngcobo, Journalist and Content Strategist March 16, 2026
written by Nokuthula Ngcobo, Journalist and Content Strategist

Parents are urged to check their cupboards after the latest Clicks recall, which has been announced for a toddler snack sold in stores and online after a specific batch tested positive for non-pathogenic Listeria contamination.

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In a statement on Sunday, 15 March, the National Consumer Commission (NCC) said the affected product is Made 4 Tots Puffs Corn Chicken 12g, supplied by Clicks Retailers Pty Limited.

According to the NCC, the recall affects 1,152 units, with 348 units sold to consumers and 804 units removed from shelves. The affected products were sold at Clicks stores in South Africa, through Clicks Online and were also distributed to Lesotho. Consumers who have the affected product are being urged not to consume it and to return it to any Clicks store for a full refund or replacement, with or without proof of purchase.

Which Product is Affected by the Clicks Recall?

This recall applies to one specific batch, not the full Made 4 Tots range. In its statement, the NCC said parents and caregivers should check the following details on the packaging:

  • Identifying number: 396194
  • MGF: 03.03.26
  • Lot: 6:003
  • Best before: 02.03.2027

The NCC said Clicks informed the regulator that the affected batch “tested positive for non-pathogenic Listeria contamination.” The supplier also noted that the type of Listeria involved is “generally non-pathogenic to humans but has rare and isolated reports of human disease.”

What is Listeria?

The word “Listeria” is enough to worry any parent, especially in South Africa, but context matters. The National Institute for Communicable Diseases (NICD) explains that listeriosis is a serious bacterial disease caused by Listeria monocytogenes. According to the National Department of Health, the bacteria can be found in soil, water and contaminated food.

The NICD says listeriosis can cause symptoms ranging from gastroenteritis to severe illness, especially in vulnerable groups. In people with weakened immune systems, it can lead to meningitis or septicaemia, while in pregnant women, it can cause pregnancy loss or infection in newborn babies.

It is important to note that this Clicks recall relates to non-pathogenic Listeria, not a confirmed case of Listeria monocytogenes. Still, the product has been recalled as a precaution and parents are being advised not to take chances.

NCC Says Suppliers Must Remove Unsafe Products Quickly

The recall was announced on World Consumer Rights Day, which this year carried the global theme “Safe Products. Confident Consumers.” In the same NCC statement, Acting Commissioner Hardin Ratshisusu reminded suppliers of their obligations under the law.

“As we mark World Consumer Rights Day today with the global theme Safe Products. Confident Consumers, we remind suppliers of their obligation to provide goods of good quality, free of defects, usable and durable,” Ratshisusu said.

He added that where goods fail to meet required standards, “those goods must be removed from the shelves to minimise potential harm.”

The NCC also said it is monitoring this recall and other recent recalls to ensure full compliance with the Consumer Protection Act.

For parents, the safest next step is to check the batch details carefully and return the product immediately if it matches the recall notice.

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Peanut Butter Recall in South Africa Over Dangerous Toxins
Health & WellnessIn The NewsYour Health

Peanut Butter Recall in South Africa Over Dangerous Toxins

by Nokuthula Ngcobo, Journalist and Content Strategist February 11, 2026
written by Nokuthula Ngcobo, Journalist and Content Strategist

The National Consumer Commission (NCC) has announced a peanut butter recall affecting specific batches of ButtaNutt products in South Africa after routine testing revealed aflatoxin levels above the legal limit.

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In its official statement this week, the NCC urged consumers to stop consuming the affected products immediately and return them to the point of purchase for a full refund.

“Consumers are advised to immediately stop consuming the identified products and return them to the retailer for a refund,” the statement read.

The commission confirmed that it is investigating the source of contamination and monitoring the recall process under the Consumer Protection Act.

What Is Aflatoxin?

Aflatoxin is a naturally occurring toxin produced by certain moulds that grow on food crops such as peanuts and maize. While trace amounts are often unavoidable, high levels can cause nausea, vomiting and abdominal pain. Long-term exposure has been linked to more serious health conditions.

The NCC explained that the presence of aflatoxin above the legal threshold triggered the peanut butter recall. This is part of South Africa’s broader food safety framework, which requires manufacturers to meet strict standards to protect consumers.

ALSO READ: Nestlé Recalls Baby Formula in South Africa After Toxin Concerns

Affected Batch and Recall Details

The peanut butter recall covers products manufactured on 15 January 2026. The affected items include ButtaNutt’s 100% Peanut (1kg and 2.5kg) and Chocolate Peanut (250g). The products have expiry dates of 13 July 2027, 15 July 2027, 17 July 2027, or 28 July 2027. These batches were distributed in Gauteng, KwaZulu-Natal, Eastern Cape and Western Cape, reaching shelves in major retailers such as Spar, Pick n Pay and Jackson’s Real Food Market.

According to a statement released by ButtaNutt, most of the affected stock has been secured and removed from the market. However, the company, based in Paarl in the Western Cape, highlighted that 83 individual units remain with consumers.

Health Risks

Providing context on the health risks to consumers who may have already consumed a portion of the affected products, ButtaNutt said: “Health experts distinguish between ‘acute’ (once-off) exposure and ‘chronic’ (long-term) exposure. Primary risks, such as liver health concerns, are typically linked to regular, long-term ingestion over decades. Scientific guidelines suggest that an adult would generally need to consume over 2.4 kg of contaminated peanut butter (at levels of 500 ppb) at least three times a week to potentially experience acute toxic effects. Consumption of a standard serving is considered a once-off exposure and is highly unlikely to cause immediate or severe health effects.”

What Consumers Should Do

  • Check your pantry: Look for ButtaNutt peanut butter products manufactured on 15 January 2026.
  • Stop consumption immediately: Do not take chances with affected batches, even if the product looks or smells normal.
  • Return for a refund: Retailers are obliged to accept the recalled items and provide a full refund.
  • Stay informed: Follow updates from the NCC and trusted news outlets for further developments.

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Broader Context of Food Safety

While the ButtaNutt recall may cause inconvenience, it is ultimately a protective measure. Consumers should see it as part of a broader effort to ensure that the products we trust are held to the highest standards.

By returning affected products and staying informed, households can navigate this peanut butter recall with confidence. Peanut butter may be a household favourite, but safety must always come first.

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Nestlé Recalls Baby Formula in South Africa After Toxin Concerns
BabiesBaby Health

Nestlé Recalls Baby Formula in South Africa After Toxin Concerns

by Nokuthula Ngcobo, Journalist and Content Strategist January 8, 2026
written by Nokuthula Ngcobo, Journalist and Content Strategist

Nestlé has announced a precautionary recall of a batch of its NAN Special Pro HA 800g infant formula in South Africa after concerns about possible contamination with cereulide, a toxin produced by certain strains of Bacillus cereus.

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The recall was confirmed on Wednesday, 7 January 2026, by the National Consumer Commission (NCC), which urged parents and caregivers to return affected products to the point of purchase for a full refund.

Affected Batch and Nestlé Recall Details

The batch in question was manufactured on 15 June 2025, has a best-before date of 15 December 2026 and was distributed across South Africa, Namibia and Eswatini. It carries the batch number 51660742F3 and is intended for infants aged zero to twelve months. 

In a statement to BabyYumYum, Nestlé South Africa said: “If you have NAN Special Pro HA 0–12 800 g tin with batch 51660742F3, please contact our Consumer Services (South Africa): +27 86 009 6116. Our team will advise on the appropriate next steps and support you with any questions.” 

No Illnesses Have Been Confirmed

On 7 January, Nestlé’s official global website released a statement. The Swiss food giant explained the background to the recall, citing a quality issue with an ingredient supplied by one of its major partners.

The company said: “Following the detection of a quality issue with an ingredient provided by a leading supplier, Nestlé has undertaken testing of all arachidonic acid (ARA) oil and corresponding oil mixes used in the production of its potentially affected infant nutrition products.

Nestlé further emphasised that the recall is precautionary and that no illnesses have been reported to date.

“No illnesses have been confirmed in connection with the products involved to date.”

It also explained that symptoms to look out for are severe or persistent vomiting, diarrhoea, or unusual lethargy. These would typically appear between 30 minutes to six hours after any exposure.

“Nestlé assures parents and caregivers that it is implementing appropriate actions to help ensure the health and wellbeing of families and their babies. At the same time, we are working to minimise any potential supply disruption,” the company said.

What Is Cereulide?

The NCC confirmed that the Nestlé recall was triggered by the identification of cereulide in the ingredient mix. Cereulide is a bacterial toxin that can cause foodborne illness, typically presenting as nausea, vomiting and stomach cramps within hours of exposure.

Nestlé acknowledged this in its advisory, saying: “Cereulide is a substance of bacterial origin that causes foodborne illness and is created by certain strains of the microorganism, Bacillus cereus. The presence of cereulide in oils is very uncommon, and Nestlé is working with the oil supplier, who is conducting a full root-cause analysis.”

Impact on Families and Global Context

The Nestle recall in South Africa forms part of a wider global withdrawal of infant formula products, including SMA, BEBA, NAN and Alfamino ranges, across at least 37 countries in Europe, Africa, Asia and the Americas. Nestlé confirmed that the batches involved represent less than 0.5% of its annual group sales, meaning the financial impact is expected to be limited.

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Media Alert: Recall of YAZ PLUS Tablets
In The NewsLifestyle

Media Alert: Recall of YAZ PLUS Tablets

by Press Release November 22, 2024
written by Press Release

Johannesburg, South Africa – November 21, 2024: Bayer (Pty) Ltd, in close consultation with the South African Health Products Regulatory Authority (SAHPRA), is issuing a medicine recall, classified as Class II, Type A, for a specific batch (WEW96J) of YAZ PLUS Tablets.

Reason for Recall:

The recall has been initiated due to the discovery of a limited number of YAZ PLUS packs from Batch WEW96J in retail pharmacies with a mix-up in the sequence of hormone-containing and hormone-free tablets.

The affected packs contain:
• 24 light orange hormone-free tablets, and
• 4 pink film-coated hormone tablets,

instead of the correct arrangement of:
• 24 pink film-coated hormone tablets, and
• 4 light orange hormone-free tablets.

Mix-up of arrangement:

YAZ Contraceptives recalled in South Africa due to packaging mix-up

This mix-up has resulted in some packs containing only 4 hormone tablets instead of the required 24, compromising the product’s contraceptive efficacy.

Batch Information:

The recall only affects Batch WEW96J of YAZ PLUS Tablets, with an expiry date of March 2026.

Action Required:

  1. Healthcare professionals, wholesalers, hospitals, retail pharmacy outlets, doctors, nurses, pharmacists, authorized prescribers, dispensers, and individual customers or patients in possession of the affected Batch can return product to their Healthcare facility from which it was dispensed, for credit.
  2. If you are in possession of YAZ PLUS tablets from the affected batch, you are urged to:
    Stop Use Immediately: If you have been taking the tablets from a batch that is affected with the mix-up, stop taking them immediately and contact your healthcare professional. While only a limited number of packs from the respective batch is affected, as a precautionary measure, no tablets from these packs shall be used until you have consulted your Healthcare Practitioner, as they may potentially not provide the contraceptive protection you expect.
  3. Return the Product: Please return any affected packs to the pharmacy or retailer where you purchased them for a replacement or refund.
  4. Check Your Packs: If you have multiple packs of YAZ PLUS, please check each one of them, to ensure they are not from the affected batch.
  5. Consult Healthcare Provider: If you have consumed tablets from the affected batch, or if you have concerns about your contraceptive coverage, please consult your healthcare provider as soon as possible for advice.

Bayer (Pty) Ltd takes the safety and efficacy of its products seriously and is committed to ensuring that all YAZ PLUS tablets in the market meet the highest quality standards. The root cause for the mix-up of tablets in the packaging has been identified and corrective measures have been implemented. This incident is limited to only this one batch and no other batches are impacted. The company is working diligently with SAHPRA and healthcare providers to facilitate the recall process and minimize any inconvenience to our customers.

Bayer (Pty) Ltd is dedicated to addressing this issue promptly and ensuring the continued health and safety of all our customers.

Further Information and Support:

For more information about this recall, or if you have any questions or concerns, please contact Bayer +27 (0) 11 921 5000. Their team is available to provide the support and information you need.

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