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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.
129 recalls in the past week from 18 countries
2,091 recalls match · Clear filters · Checked 2 minutes ago
United StatesHamilton Medical AG recalls IntelliCuff
Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error.BD Switzerland Sarl recalls MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461…
Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S.Medacta Usa Inc recalls Short Monobloc Stem Broaches
Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem…Laborie Medical Technologies Corp recalls Solar GI System
Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing…Medline Industries, LP recalls Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH
Expansion of RES 98277.Medtronic Heart Valves Division recalls Medtronic Harmony Delivery Catheter System
Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under…Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console.Depuy (Ireland) recalls Depuy Synthes and 1 more products
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.Siemens Medical Solutions USA, Inc recalls ARTIS icono biplane. Model Number: 11327600. and 2 more products
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.Zimmer Surgical Inc recalls Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems… and 1 more products
Potential sterility breach in sealing area of sterile pouch.Windstone Medical Packaging, Inc. recalls A M S and 3 more products
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine…Baxter Healthcare Corporation recalls Adapter for Head Positioning
The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of the…Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console.Hamilton Medical AG recalls Breathing circuit set
Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which will result…W L Gore & Associates, Inc. recalls GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers
Due to catheter separationMentor Texas LP recalls SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe
A single lot of expired syringes were distributed due to a distribution system control failure.Covidien LLC recalls Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060…
Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.Medela Inc recalls Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog…
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible.Siemens Medical Solutions USA, Inc recalls ARTIS icono ceiling. Model Number: 11328100.
Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place.Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT and 3 more products
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits.Insulet Corporation recalls Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2.… and 2 more products
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus…Carl Zeiss Meditec AG recalls Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.Masimo Corporation recalls Radius VSM ECG pre-connected Set and 1 more products
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal…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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