Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,836 recalls, newest first · Checked 18 minutes ago
United Statesembecta Medical II LLC recalls EWO_02512 and 1 more products
Retrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices.AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE REF: KRIV26-02
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioidesBard Access Systems, Inc. recalls Power-Trialysis Short-Term Straight Dialysis Catheter and 1 more products
this is a downstream recall of class I recall RES 98777PTW Freiburg recalls Brand Name: VERIQA
When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead…Noxbox LTD recalls NOxBOXi Nitric Oxide Delivery System.
Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation.Medline Industries, LP recalls Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A and 3 more products
Kits may exhibit open seals in sterile pouch packaging.Boston Scientific Corporation recalls Boston Scientific Corporation StoneSmart Connect Console Contents:
A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path.Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit and 2 more products
The packaging may not consistently maintain sterile barrier integrity.Wilson-Cook Medical Inc. recalls Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT…
Due to issue with endoscope adherence and inability to spray powder.Bayer Medical Care, Inc. recalls MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System
Some devices may not have been properly sterilized due to a manufacturing sterilization issue.Pi Cardia LTD recalls Pi-Cardia Inc. ShortCut REF: Z-A-20.003-US
Transfemoral catheter, positing arm may detached due to weld issue.Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System
Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from…F & A Foundation recalls Reign Medical Clench Staple System
Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established.Howmedica Osteonics Corp. recalls AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No. C-M112-2-500 Orthopaedic implant… and 11 more products
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.Philips North America recalls Philips Patient Information Center iX REF:866389 and 1 more products
Due to software malfunction, patient information system may freeze and become unresponsive.Abiomed, Inc. recalls Automated Impella Controller and 2 more products
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.GE Healthcare recalls Centricity Enterprise Archive V2 and 5 more products
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient.Happiest Baby, Inc recalls Happiest Baby and 1 more products
Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA.Medline Industries, LP recalls Medline Convenience Kit: OPEN HEART A PACK
The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach.ICU Medical, Inc. recalls Plum administration sets and 3 more products
Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC)…Nova Biomedical Corporation recalls StatStrip Glucose Hospital Meter System. Model No: 63685. Glucose test system. and 4 more products
A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously…GE Medical Systems Information Technologies Inc recalls Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04
Device may not resume patient monitoring for at least 3 minutes following system restart.Medline Industries, LP recalls Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET and 6 more products
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth…A little guidance
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Recall classes explained: Class I, II and III
What the FDA's recall classes, Canada's classes and types, and UK and EU alert levels mean, with how often each one comes up.
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How to check if your car has a recall
Find the recalls for your make and model, confirm with your VIN whether your car is affected, and know what do-not-drive and park-outside warnings mean.
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What to do if something you own is recalled
Refunds, repairs, replacements and proof of destruction: what to expect, and how to handle recalled food, medicines, batteries and children's products safely.