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.
Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used with EG-3670URK and EG-3870UTK ultrasound gastroscopes. In the disinfection step, the IFU has a warning…
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Potential inaccurate calibration by service depot repair, which could contribute to patients being burnt by the device. This only impacts units serviced between the dates of 09/08/2016 and…
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Potential inaccurate calibration by service depot repair, which could contribute to patients being burnt by the device. This only impacts units serviced between the dates of 09/08/2016 and…
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Some ORA Carts have the potential to return an incorrect IOL power measurement during cataract surgery. This issue appears to have been caused by a software coding error that results in the…
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used with EG-3670URK and EG-3870UTK ultrasound gastroscopes. In the disinfection step, the IFU has a warning…
The firm manufactured and distributed custom surgical kits which contained BD SafetyGlide" 22GA 1 inch Needles. BD subsequently recalled these needles because, " Loose polypropylene…
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Medtronic received reports that the DBS depth stop did not adequately secure to the lead, which can result in DBS lead placement beyond the intended target.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Some ORA Carts have the potential to return an incorrect IOL power measurement during cataract surgery. This issue appears to have been caused by a software coding error that results in the…
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Undeclared yellow # 5
Undeclared allergens: Butter fails to disclose the presence of milk and ice cream sandwiches fail to disclose the presence of wheat.
Product is recalled due to potential contamination with E.coli O26.
Browse recent months with enough recall history for useful comparison.
