Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Possible prevention of high and low voltage therapy in Medtronic Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillator (CRT-D).
Vygon is conducting a voluntary recall of the products and lots listed in this recall, being initiated because our Tyvek supplier has notified Vygon of issues with their product,…
There is a potential for the devices to create staples that do not meet formed staple height specifications which can result in malformed staples.
Complaints were filed claiming the material consistency was too soft and too sticky in comparison to its usual consistency, causing unexpected handling for the user during packing and…
Knee implant components (tibial bearings) are labeled with the incorrect size.
FUJIFILM Medical Systems U.S.A., Inc. (FMSU) identified a potential failure with our Mammography system. The acquisition workstations, FDR¿1000AWS, FDR-2000AWS, FDR-3000AWS, and CR¿IR363AWS…
Vygon is conducting a voluntary recall of the products and lots listed in this recall, being initiated because our Tyvek supplier has notified Vygon of issues with their product,…
Rapid fFN cassettes were manufactured with material (A137 ascites) from a new supplier (SDIX). The products were distributed to customers before FDA approved the change to use the material…
The duodenoscopes are being recalled in order to replace the forceps elevator mechanism, the O-rings, and the distal end covering to be consistent with the updated design as well as provide…
Vygon is conducting a voluntary recall of the products and lots listed in this recall, being initiated because our Tyvek supplier has notified Vygon of issues with their product,…
The base of the frame has the potential to crack when the patient is initially transferred to the Bow Frame.
Nine lots of 8.5 mm Polyaxial Pedicle Screws are at risk of breakage.
The product is labeled with the incorrect expiration date.
After multiple reprocessing cycles, the epoxy resin which holds the TCN Electrode in the hub can exhibit signs of damage. In some cases, this damage may result in the inability to fully…
Robot arm being sent to the wrong position
Possible sterile barrier breach in the pouch of Affinity NT Cardiotomy Venous Reservoir stand alone uncoated and Affinity NT Cardiotomy Venous Reservoir stand alone Trillium coated products.
Firm was notified of a positive test result for Listeria monocytogenes.
The firm was notified by the Ohio Dept. of Agriculture (ODA) of insufficient pasteurization monitoring measures.
Frozen blend vegetable product containing green beans are recalled due to a potential contamination with Listeria monocytogenes.
Aryzta LLC is recalling multiple lots of bread dough following a supplier's recall of a yeast ingredient due to potential contamination with metal fragments.
Product is uneviscerated and has the potential to be contaminated with Clostridium botulinum.
The firm was notified by the Ohio Dept. of Agriculture (ODA) of insufficient pasteurization monitoring measures.
Frozen green beans are recalled due to a potential contamination with Listeria monocytogenes.
Organic Creamy Wheat Hot Cereal is recalled due to undeclared wheat. The front label is correctly labeled as Organic Creamy Wheat Hot Cereal. However, the back label is mistakenly labeled…
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