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.
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Potential for the sheath tip on the biopsy needle to separate from the sheath shaft.
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021,FDA published a Letter to Health Care Providers to further…
Under certain conditions, there is a risk for a false negative result.
Units may arrive with missing pins and/or in a state in disassembly. Pins dislodging from the instrument during a procedure may enter the surgical cavity, requiring intraoperative removal…
Software 2.51 and Lower with Installed CO2 Measurement Option, may result in Restart of the Ventilator, brief cessation of ventilation can occur and loss of PEEP for approx. 8 seconds
Engraving on implants may not match what is listed on the pouch labels.
There is a risk that the Diode D1 in the Modulator can fail in a destructive manner when removed from the machine, and that the protective tube surrounding the diode may fail to contain the…
False Mutation Detected results for the exon 20 insertion (Ex20Ins) mutation when using the cobas EGFR Mutation Test v2, may lead to inappropriate treatment
There is a risk that the Diode D1 in the Modulator can fail in a destructive manner when removed from the machine, and that the protective tube surrounding the diode may fail to contain the…
Engraving on implants may not match what is listed on the pouch labels.
There is a potential for false positive results.
Customers were not notified of previous recalls associated with various defibrillator models.
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Undeclared anchovies.
Product has potential for spoilage and lack of commercial sterility.
Potential non-O157 STEC (Shiga-Toxin 1) contamination. Serotype OXY31:H20 (stx1a with saa)
Product was recalled due to the presence of undeclared wheat.
European customer reported that berries received from this grower was found to include a few small metal spheres, about 2.45 mm diameter.
Undeclared egg
Potentially contaminated with E. Coli
SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected powder substance. There was also a lack of full drug effect upon administration.
Volkswagen Group of America, Inc. (Audi) is recalling certain 2021 Audi A8 and S8, 2022 Audi A5 Sportback, A4 Sedan, E-Tron GT, Q3, Q5, RS6 Avant, A3 Sedan, S5 Sportback, Q5 Sportback, Q7,…
Browse recent months with enough recall history for useful comparison.
