Office for Product Safety and Standards · July 24, 2026
- Affected product
- Product Safety Report: PCL Push Button Safety (PBS) Coupling
- Category
- Consumer product recalls
- Hazard
- of injuries. From: Office for Product Safety and Standards
Check affected Product Safety Report: PCL Push Button Safety (PBS) Coupling identifiers →Medicines and Healthcare products Regulatory Agency · July 23, 2026
- Affected product
- Class 4 Medicines Defect Notification: Neuraxpharm UK Ltd, Tuzulby
- Category
- Medical device recalls
- Hazard
- Neuraxpharm UK Ltd has informed the MHRA of missing safety information in the Patient Information Leaflet (PIL) and Summary of Product Characteristics (SmPC) for certain batches of Tuzulby prolonged release 20mg, 30mg and 40mg chewable tablets.
Check affected Class 4 Medicines Defect Notification: Neuraxpharm UK Ltd, Tuzulby identifiers →Food Standards Scotland · July 22, 2026
- Affected product
- Food alert 22 July 2026 Graham’s Family Dairy Graham’s Family Dairy
- Category
- Food recalls
- Hazard
- The presence of veterinary medicines, including antibiotics in the product may make it unsafe to consume and may be a possible health risk for anyone with an allergy to antibiotics including penicillin. Our advice to consumers: If you have bought the above…
Check affected Food alert 22 July 2026 Graham’s Family Dairy Graham’s Family Dairy identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : Wizz Toys Squishy Sausage Dog (2607-0186)
- Category
- Baby product recalls, Pet food recalls, Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Wizz Toys Squishy Sausage Dog (2607-0186) identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : 32cm Standing Gingerbread Doorstops (2607-0175)
- Category
- Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : 32cm Standing Gingerbread Doorstops (2607-0175) identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : Snow White 27cm Standing Gingerbread Doorstops (2607-0177)
- Category
- Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Snow White 27cm Standing Gingerbread Doorstops (2607-0177) identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : Wizz Toys 15cm Nana Banana Stress Toy (2607-0009)
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Wizz Toys 15cm Nana Banana Stress Toy (2607-0009) identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : Wizz Toys Jumbo Mr Splat Stretch Men (2607-0181)
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Wizz Toys Jumbo Mr Splat Stretch Men (2607-0181) identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : Wizz Toys Squishy Sand Yeti Monsters (2607-0183)
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Wizz Toys Squishy Sand Yeti Monsters (2607-0183) identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : Wizz Toys 6.5cm Decorative Wishing Bottle (2607-0182)
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Wizz Toys 6.5cm Decorative Wishing Bottle (2607-0182) identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : Haunted House Jumbos and Filled Critters Toys (2607-0185)
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Haunted House Jumbos and Filled Critters Toys (2607-0185) identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : Wizz Toys 7.5cm x 4cm Shells Decorative Wishing Bottle
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Wizz Toys 7.5cm x 4cm Shells Decorative Wishing Bottle identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : Wizz Toys 13.5cm Dino Sand Stretchy Racers (2607-0179)
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Wizz Toys 13.5cm Dino Sand Stretchy Racers (2607-0179) identifiers →Food Standards Scotland · July 21, 2026
- Affected product
- Food alert 21 July 2026 Farmfoods packs of 8 Farmfoods Quarter
- Category
- Food recalls
- Hazard
- Causes of food poisoning Food incidents Food crime Contaminants in food Novel foods Buying food on social media Food labels Food labels Use by and best before date labels Nutritional labels Food Hygiene Information Scheme Know the food facts Know the food…
Check affected Food alert 21 July 2026 Farmfoods packs of 8 Farmfoods Quarter identifiers →Office for Product Safety and Standards · July 21, 2026
- Affected product
- Product : Wizz Toys Squishy Puppies (2607-0184)
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Wizz Toys Squishy Puppies (2607-0184) identifiers →Medicines and Healthcare products Regulatory Agency · July 20, 2026
- Affected product
- Class 4 Medicines Defect Notification: Macarthys Laboratories Ltd
- Category
- Medical device recalls
- Hazard
- Macarthys Laboratories Ltd T/A Martindale Pharma has notified the MHRA of a manufacturing issue impacting several batches of Xaggitin XL Prolonged-release Tablets, due to the occurrence of incorrect tablet counts in the bottles.
Check affected Class 4 Medicines Defect Notification: Macarthys Laboratories Ltd identifiers →Office for Product Safety and Standards · July 20, 2026
- Affected product
- Product : Chick C Toy sold via Amazon (2602-0270)
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- of choking and burns. From: Office for Product Safety and Standards
Check affected Product : Chick C Toy sold via Amazon (2602-0270) identifiers →Office for Product Safety and Standards · July 15, 2026
- Affected product
- Product : Juncture Water Beads (50,000 Pcs) sold via Amazon
- Category
- Consumer product recalls
- Hazard
- of asphyxiation. From: Office for Product Safety and Standards
Check affected Product : Juncture Water Beads (50,000 Pcs) sold via Amazon identifiers →Medicines and Healthcare products Regulatory Agency · July 13, 2026
- Affected product
- Class 2 Medicines : Beckton Dickson UK Ltd, ChloraPrep 1mL
- Category
- Medical device recalls
- Hazard
- Becton Dickinson UK Ltd are recalling batches of ChloraPrep 2% w/v / 70% v/v cutaneous solution 1mL applicators due to a potential breach of sterility in the packaging process.
Check affected Class 2 Medicines : Beckton Dickson UK Ltd, ChloraPrep 1mL identifiers →Medicines and Healthcare products Regulatory Agency · July 9, 2026
- Affected product
- Class 2 Medicines : Bristol Laboratories Limited
- Category
- Medical device recalls
- Hazard
- Bristol Laboratories Limited is recalling one batch (7124002) of Phenoxymethylpenicillin 250 mg/5 ml Oral Solution Sugar Free due to product labelling issues.
Check affected Class 2 Medicines : Bristol Laboratories Limited identifiers →Medicines and Healthcare products Regulatory Agency · June 30, 2026
- Affected product
- Class 3 Medicines : Flamingo Pharma UK Ltd, Flucloxacillin Capsules
- Category
- Medical device recalls
- Hazard
- Flamingo Pharma UK Ltd have informed the MHRA that certain packs of Flucloxacillin Capsules BP 500mg contain the incorrect PIL. The affected packs contain the PIL for Amoxicillin 500mg Capsules instead of the PIL for Flucloxacillin BP 500mg Capsules.
Check affected Class 3 Medicines : Flamingo Pharma UK Ltd, Flucloxacillin Capsules identifiers →Medicines and Healthcare products Regulatory Agency · June 30, 2026
- Affected product
- UPDATE: Class 4 Medicines Defect Notification: Relonchem Limited
- Category
- Medical device recalls
- Hazard
- Relonchem Limited have informed the MHRA that particles have been observed inside some bottles of Gabapentin Relonchem Oral Solution, identified through a customer complaint.
Check affected UPDATE: Class 4 Medicines Defect Notification: Relonchem Limited identifiers →Medicines and Healthcare products Regulatory Agency · June 29, 2026
- Affected product
- Class 4 Medicines Defect Notification: Brancaster Pharma Limited
- Category
- Medical device recalls
- Hazard
- Brancaster Pharma Limited has informed the MHRA that the Patient Information Leaflet (PIL) in the cartons for the batches listed in this notification were released with an outdated PIL.
Check affected Class 4 Medicines Defect Notification: Brancaster Pharma Limited identifiers →Medicines and Healthcare products Regulatory Agency · June 16, 2026
- Affected product
- Class 3 Medicines : Orbit Pharma Limited, Cyclizine Lactate 50 mg/ml
- Category
- Medical device recalls
- Hazard
- Orbit Pharma Limited is recalling a specific batch of Cyclizine Lactate 50 mg/ml Solution for injection as a precautionary measure due to Good Manufacturing Practice (GMP) deficiencies identified at the manufacturing site.
Check affected Class 3 Medicines : Orbit Pharma Limited, Cyclizine Lactate 50 mg/ml identifiers →Medicines and Healthcare products Regulatory Agency · June 8, 2026
- Affected product
- Class 4 Medicines Defect Notification: Cadila Pharmaceuticals
- Category
- Medical device recalls
- Hazard
- Cadila Pharmaceuticals Limited has informed the MHRA of an error with the European Article Number (EAN) barcode on the cartons of a batch of Mirtazapine 30mg Film-Coated Tablets distributed in Crescent Pharma Limited livery.
Check affected Class 4 Medicines Defect Notification: Cadila Pharmaceuticals identifiers →Medicines and Healthcare products Regulatory Agency · June 4, 2026
- Affected product
- Class 4 Medicines Defect Notification: Teva UK Ltd, Ponlimsi
- Category
- Medical device recalls
- Hazard
- Teva UK Limited is reporting a labelling error on the carton for Ponlimsi (Denosumab) 60mg Solution for injection in Pre-filled Syringe. The carton states “For application to the skin” when the product is licensed for subcutaneous use.
Check affected Class 4 Medicines Defect Notification: Teva UK Ltd, Ponlimsi identifiers →Medicines and Healthcare products Regulatory Agency · June 2, 2026
- Affected product
- Class 2 Medicines : Becton Dickinson UK Ltd, ChloraPrep 2% 1mL and
- Category
- Medical device recalls
- Hazard
- Becton Dickinson UK Ltd are recalling batches of ChloraPrep 2% 1mL applicators and ChloraPrep Frepp 2% 1.5 mL applicators due to a potential breach of sterility in the packaging process.
Check affected Class 2 Medicines : Becton Dickinson UK Ltd, ChloraPrep 2% 1mL and identifiers →Medicines and Healthcare products Regulatory Agency · May 28, 2026
- Affected product
- Class 2 Medicines : Crescent Pharma Limited, Ramipril 2.5 mg
- Category
- Medical device recalls
- Hazard
- Crescent Pharma Limited is initiating a precautionary recall of one batch of Ramipril 2.5 mg Capsules following the identification of a potential packaging error at the manufacturing site.
Check affected Class 2 Medicines : Crescent Pharma Limited, Ramipril 2.5 mg identifiers →Medicines and Healthcare products Regulatory Agency · May 27, 2026
- Affected product
- Allurion Gastric Balloon: Updated safety information the risks of
- Category
- Medical device recalls
- Hazard
- In rare instances, the Allurion Gastric Balloon has not transited through the stomach or bowel as intended, leading to complications such as gastric outlet obstruction, small bowel obstruction and gastric perforation.
Check affected Allurion Gastric Balloon: Updated safety information the risks of identifiers →Medicines and Healthcare products Regulatory Agency · May 20, 2026
- Affected product
- severe harm from use of incorrect giving (administration) set for
- Category
- Medical device recalls
- Hazard
- There is a potential for serious harm to patients if an intravenous (IV) infusion giving set is used instead of a blood transfusion giving set to deliver a transfusion of blood or blood components.
Check affected severe harm from use of incorrect giving (administration) set for identifiers →Medicines and Healthcare products Regulatory Agency · May 19, 2026
- Affected product
- Kimal Procedure Packs containing recalled components: Namic
- Category
- Medical device recalls
- Hazard
- Medline Industries LP and Kimal PLC have identified safety issues with the Namic Angiographic Control Syringes with RA and Namic White Star Off Handle Manifold devices, and have issued field safety notices to affected UK hospitals advising that they should not…
Check affected Kimal Procedure Packs containing recalled components: Namic identifiers →Medicines and Healthcare products Regulatory Agency · May 14, 2026
- Affected product
- Class 4 Medicines Defect Notification: Fresenius Medical Care
- Category
- Medical device recalls
- Hazard
- Fresenius Medical Care Deutschland GmbH have identified an error in the Braille printed on the outer label.
Check affected Class 4 Medicines Defect Notification: Fresenius Medical Care identifiers →Medicines and Healthcare products Regulatory Agency · May 11, 2026
- Affected product
- Class 4 Medicines Defect Notification: Milpharm Limited, Loperamide
- Category
- Medical device recalls
- Hazard
- Milpharm Limited has identified a discrepancy in the Patient Information Leaflet (PIL) approved for Loperamide hydrochloride 2 mg Orodispersible Tablets.
Check affected Class 4 Medicines Defect Notification: Milpharm Limited, Loperamide identifiers →Medicines and Healthcare products Regulatory Agency · April 28, 2026
- Affected product
- Class 2 Medicines : Amarox Limited, Sertraline 100mg film-coated
- Category
- Medical device recalls
- Hazard
- of more pronounced serotonergic effects. The risk is however higher in patients with pre-existing cardiac conditions, those aged over 65 years, or those taking concomitant serotonergic or QT prolonging medication. Additionally, as some patients may require…
Check affected Class 2 Medicines : Amarox Limited, Sertraline 100mg film-coated identifiers →Medicines and Healthcare products Regulatory Agency · April 23, 2026
- Affected product
- Class 3 Medicines : Omega Pharma Ltd, Napralief 250mg
- Category
- Medical device recalls
- Hazard
- with this page
Check affected Class 3 Medicines : Omega Pharma Ltd, Napralief 250mg identifiers →Medicines and Healthcare products Regulatory Agency · April 22, 2026
- Affected product
- Class 4 Medicines Defect Notification: Doncaster Pharma Limited
- Category
- Medical device recalls
- Hazard
- of dosing errors arising from the Braille issue. Advice for Patients: No action is needed from patients, continue to take medication from these batches of tablets. The actions will be controlled by the healthcare professionals who prescribe or dispense the…
Check affected Class 4 Medicines Defect Notification: Doncaster Pharma Limited identifiers →Medicines and Healthcare products Regulatory Agency · April 20, 2026
- Affected product
- Class 2 Medicines : Crescent Pharma Limited, Ramipril 10mg capsules
- Category
- Medical device recalls
- Hazard
- with this page
Check affected Class 2 Medicines : Crescent Pharma Limited, Ramipril 10mg capsules identifiers →Office for Product Safety and Standards · April 8, 2026
- Affected product
- Product Safety Report: Ooze Brink Sub-Ohm Dry Herb Vape (2603-0159)
- Category
- Consumer product recalls
- Hazard
- of fire. From: Office for Product Safety and Standards
Check affected Product Safety Report: Ooze Brink Sub-Ohm Dry Herb Vape (2603-0159) identifiers →Office for Product Safety and Standards · March 20, 2026
- Affected product
- Product : Texet Bright Start Coloured Crafting Sand Pack of 20
- Category
- Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Texet Bright Start Coloured Crafting Sand Pack of 20 identifiers →Office for Product Safety and Standards · March 20, 2026
- Affected product
- Product : Texet Bright Start Fluorescent Coloured Craft Sand Pack of
- Category
- Consumer product recalls
- Hazard
- to health. From: Office for Product Safety and Standards
Check affected Product : Texet Bright Start Fluorescent Coloured Craft Sand Pack of identifiers →
