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Jif recall check: lot codes 1274425-2140425 matter for UAE clinics and pharmacies

Jif recall check: lot codes 1274425-2140425 matter for UAE clinics and pharmacies

A Jif recall item raises a practical UAE question: which lots should clinics and pharmacies check, and when should patients seek care?

Zavis Intelligence·Healthcare Industry Desk
30 Aug 2026·3 min read

How Zavis verifies this coverage

Editorial standards, source rules, methodology, and review provenance are public.

Mshale carried a 30 August 2026 item headlined “Jif Issues Peanut Butter Recall Ponta Delgada,” but the actionable recall record for UAE operators remains the U.S. Food and Drug Administration notice for select Jif peanut butter products with lot codes 1274425 to 2140425 ending in 425.

The highest-stakes readers are pharmacy operations heads, clinic COOs and medical directors. Their immediate job is narrow: check stock, remove affected imported jars if found, and triage patients with possible Salmonella symptoms. In Dubai, the relevant healthcare regulator is the Dubai Health Authority (DHA), while imported food safety sits with Dubai Municipality and federal coordination through the Ministry of Climate Change and Environment (MOCCAE). In Abu Dhabi and Al Ain, clinical reporting and facility oversight sit with the Department of Health Abu Dhabi (DOH). In Sharjah, Ajman, Umm Al Quwain, Ras Al Khaimah and Fujairah, licensed healthcare providers are regulated by the Ministry of Health and Prevention (MOHAP).

What UAE operators should verify

The FDA recall was first published on 20 May 2022 by The J.M. Smucker Co. for select Jif products sold in the U.S. because of potential Salmonella contamination. The U.S. Centers for Disease Control and Prevention said the recalled products were sold worldwide and covered multiple types and sizes, including creamy, crunchy, natural and reduced-fat peanut butter.

UAE pharmacies, clinic pantries, school clinics and nutrition practices should check physical jars against the lot code near the best-before date. The recalled pattern is specific enough for staff action:

  • First four digits: 1274 to 2140.
  • Next three digits: 425.
  • Example code identified by CDC: 1352425.
  • Action: do not sell, serve or use; isolate the product and follow local recall instructions.

Operators should search supplier records by brand, product description, country of origin, lot code and invoice date. If a UAE supplier cannot provide lot-level traceability, the issue becomes a procurement control problem for the COO and a claims exposure problem for the CFO. Peanut butter sold through mainstream UAE retail channels usually costs about AED 12 to AED 35 per jar, depending on size and import channel; the bigger cost is staff time, refund handling and any patient episode that triggers consultation or laboratory testing.

Clinical and insurance exposure

The clinical risk is concentrated in children under 5, adults aged 65 and above, pregnant patients and immunocompromised patients. CDC guidance says Salmonella symptoms usually start 6 hours to 6 days after exposure and usually last 4 to 7 days. Symptoms include diarrhoea, fever, stomach cramps, nausea and vomiting.

For UAE clinics, the practical pathway is history-taking, hydration assessment and selective stool testing where symptoms are severe, prolonged or linked to a high-risk patient. Insurers such as Daman, Thiqa and Sukoon may see the episode as routine outpatient gastroenteritis unless documentation shows a foodborne cluster, admission risk or public-health reporting need. Clinics should record the brand, lot code, purchase location, symptom onset date and household exposure count in the medical record.

There is no verified UAE-wide public recall notice for this Mshale-triggered item in the sources reviewed for this article. That matters. A foreign recall does not automatically mean the same batch is on UAE shelves. It does mean procurement teams should ask distributors for batch declarations when imported ready-to-eat foods are used in clinics, staff cafeterias or dietetic programmes.

Regulatory context for Dubai first

Dubai operators should treat Dubai Municipality as the first food-safety point for imported product checks, while DHA remains the healthcare regulator for licensed clinical response. Dubai Municipality states that its Food Safety Department covers imported food products, food activities and investigation of food-borne illnesses. That gives clinic groups a clear division: the clinic manages patient care and documentation; the food-safety authority handles market control.

In Abu Dhabi, the clinical side sits with DOH. In the northern emirates, MOHAP-regulated clinics should follow MOHAP licensing and clinical reporting channels. For cross-emirate groups, the operational control should be centralised: one recall register, one supplier response template, and one clinical note prompt in the electronic medical record.

What should operators do next? Check any Jif stock today, keep photographs of labels and lot codes, ask suppliers for written batch status, and brief reception and nursing staff to escalate high-risk gastroenteritis cases within 24 hours. Patients should be told to discard matching products and seek medical advice if fever, bloody diarrhoea, dehydration or symptoms lasting more than 3 days occur.

For licensed pharmacy options in the UAE, readers should use the UAE Open Healthcare Directory to find regulated pharmacy providers before substituting products or directing patients to a dispensing location.

ZI

Zavis Intelligence

Healthcare Industry Desk

Contributing to UAE healthcare industry coverage

Source: Mshale

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A Jif recall item raises a practical UAE question: which lots should clinics and pharmacies check, and when should patients seek care?