Product Recalls in South Dakota
Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,534 recalls have been distributed to South Dakota in the last 12 months.
Showing 4781–4800 of 27,558 recalls
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custodiol HTK Solution Recalled by Dr Franz Koehler Chemie Gmbh Due to...
The Issue: Potential for particles to be present in solution.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST" Recalled by...
The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis Recalled...
The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Point of Care Control Control i-STAT¿ Level 1 10 X 1.7 mL Recalled by...
The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set...
The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.