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.
Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that…
Vibrations of the C-arm of the plane B may result in reduced image quality caused by the screw connection to the C-arm in the ceiling support
The set screw is not able to advance or reverse from the original position in the nail.
The products labeling contains inconsistencies. In certain instances, the lidstock, banner card and shipper label state that the Spring Wire Guide (SWG) within is .032 rather than the…
Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with PSVPro Spontaneous Breathing Modes do not provide the PSVPro ventilation mode feature of transitioning to SIMV PCV…
Degradation of the PGA suture material used in the manufacture of the resorbable mesh devices was observed during an on-going product stability study. Further investigation indicated that…
There is lot to lot variability for QC and patient results when using the identified reagent cartridge lots.
The set screw is not able to advance or reverse from the original position in the nail.
Vibrations of the C-arm of the plane B may result in reduced image quality caused by the screw connection to the C-arm in the ceiling support
The set screw is not able to advance or reverse from the original position in the nail.
The beds with the high rail side rail option may not be complaint with IEC 60601-2-52/C1:2010. There is a potential risk of entrapment.
Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with PSVPro Spontaneous Breathing Modes do not provide the PSVPro ventilation mode feature of transitioning to SIMV PCV…
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Firm received notification from their supplier of a voluntary recall due to the potential contamination of Salmonella and/or Listeria.
Product contains undeclared milk.
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Firm was notified by McCain Foods that the corn used in their layer dip is being recalled due to potential Salmonella/Listeria monocytogenes contamination.
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Product tested was not in compliance for pesticide exclusion.
Deli Star Inc. dba King's Food Products initiated a voluntary recall of Chef s Request professional steak marinade and Buckhead wildlife marinade due to undeclared allergens soy and wheat.
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Products may contain elevated levels of lead.
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Browse recent months with enough recall history for useful comparison.
