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Product Recalls
The latest product recalls from around the world in one place: food, cars, toys, electronics, medicines and more, from 11 government sources in the US, Canada, the UK, the EU, Australia and Asia.
119 recalls in the past week from 23 countries
2,091 recalls match · Clear filters · Checked 5 minutes ago
United StatesAniara Diagnostica LLC recalls ZYMUTEST HIA IgG
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive…Dexcom, Inc. recalls Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM… and 2 more products
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows.Quidel Corporation recalls QuickVue Dipstick Strep A Test
Product has the potential for false positive resultsStryker Corporation recalls Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The…
Due to nonconforming products being inadvertently distributed.Arrow International, LLC recalls Arrow Edge Hemodialysis Catheterization Product and 3 more products
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets.On-X Life Technologies, Inc. recalls On-X Mitral Heart Valve with Conform-X Sewing Ring
Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.Windstone Medical Packaging, Inc. recalls Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes…
Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result…Medtronic Neuromodulation recalls Medtronic SynchroMed Flex Infusion Mode
Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive…Omnicell, Inc. recalls Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028
Potential for mislabeled syringe produced by the i.v.STATION device.Hologic, Inc recalls SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC and 1 more products
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.Djo, LLC recalls Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494… and 3 more products
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.Microvention Inc. recalls LVIS Intraluminal Support Device
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration.Stryker Sustainability Solutions recalls BARD Dynamic Deca Steerable and 25 more products
Incomplete seals on sterile productGE Medical Systems, LLC recalls Revolution Ascend and 6 more products
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in…Medline Industries, LP recalls Namic Angiographic Manifold and 10 more products
Medline has identified the presence of particulate within the fluid path of the Manifolds.Ascend Laboratories, LLC recalls Ascend Laboratories
Failed Dissolution SpecificationsENDO USA, Inc. recalls Buprenorphine Hydrochloride
Crystallization; identified as Buprenorphine free baseOasis Medical, Inc. recalls Oasis Tears PF
Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.Ocinet, Inc. recalls ...And Kimchi branded kimchi
Undeclared allergen ingredient (fish)Prospector Popcorn, LLC recalls Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn
Products contain undeclared soy, specifically soy lecithin.Sugar Foods LLC recalls Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ
Possible Salmonella in croutons.Ferris Coffee and Nut Company, Inc. recalls Frederik's by meijer Vanilla Bourbon Trail Mix
Undeclared allergens (wheat and soy).Pure Ground Ingredients, Inc. recalls Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk
Product has the potential to be contaminated with Salmonella.Questions
Where do these recalls come from?
Straight from the government agencies that publish them: the CPSC, FDA and NHTSA in the United States, Health Canada, the CFIA and Transport Canada, the UK's Office for Product Safety and Standards and Food Standards Agency, the EU's Safety Gate, Product Safety Australia and Food Standards Australia New Zealand, and the OECD's GlobalRecalls portal for Korea, Japan and other countries. Every recall links to the agency's own notice.
How often is the list updated?
We check most agencies every hour and a few every 30 minutes, so a recall usually appears here within an hour or two of being published. The time of the last check is shown above the list.
How do I check if something I own has been recalled?
Search for the brand, the product name, or a model, lot or batch number from the label. Then open the recall and compare the identifying details (model numbers, UPCs, dates) with your product; a recall often covers only some batches or production dates. For a car, use the manufacturer's or the regulator's VIN lookup.
What should I do if my product has been recalled?
Follow the 'What to do' section of the recall, which comes from the official notice. Usually that means stopping use straight away and contacting the company for a refund, repair or replacement. You normally don't need a receipt, and the remedy is free.
Can I follow new recalls?
Yes. Every list has an RSS feed with the same filters, so you can follow, say, food recalls in Canada or recalls for a brand you own in any feed reader.
About
Check whether something you own has been recalled, and follow new recalls as they’re published. We collect recalls and safety alerts from government agencies around the world every hour and put them in one searchable list, newest first.
Every recall gets its own page: what’s affected and how to identify it (models, lot codes, UPCs, dates), the hazard, what to do, where it was sold, and a link to the official notice. Browse by category or country, or follow any list with RSS.
How it works
- Straight from the source. Recalls come from the CPSC, FDA and NHTSA (US), Health Canada, the CFIA and Transport Canada, the UK’s Office for Product Safety and Standards and Food Standards Agency, the EU’s Safety Gate, Product Safety Australia, Food Standards Australia New Zealand, and the OECD’s GlobalRecalls portal for Korea, Japan and other countries.
- Checked every hour. A few agencies are checked every 30 minutes, so most recalls appear within an hour or two of publication.
- Search by what’s on the label. Brand, product name, model number, batch or lot code.
- Sorted for you. Each recall is filed under a category (food, vehicles, kids and baby, electrical, health and beauty, home) and tagged with its hazards, such as fire, choking or undeclared allergens.
Notes
Recall notices are summarised from the agencies’ official data, and every page links to the original. Always check the official notice before acting on a recall. LabAnvil isn’t affiliated with any of the agencies listed.
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