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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 28681–28700 of 47,632 recalls
Recalled Item: Venture RX Catheter Recalled by Vascular Solutions, Inc. Due to Vascular...
The Issue: Vascular Solutions, Inc. (VSI) is voluntarily removing all lots of Venture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pereyra-Raz Ligature Carrier Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stamey Needle Recalled by Cook Inc. Due to reprocessing instructions do not...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pereyra Ligature Carrier 75 Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatLock¿ IV Premium Catheter Stabilization Device Recalled by Bard Access...
The Issue: StatLockTM IV Premium Catheter Stabilization Device may contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips V60 Ventilators Recalled by Respironics California Inc Due to Over...
The Issue: Over time, low-frequency vibrations can cause the pins within the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brennen Skin Graft Mesher. Surgical instrument designed to expand skin...
The Issue: Sterilization validation failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: There is a possibility of a data acquisition disruption that may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: There is a possibility of a data acquisition disruption that may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microalbumin Reagent Recalled by Beckman Coulter Inc. Due to Beckman Coulter...
The Issue: Beckman Coulter has confirmed that MA Reagent Lot M609458 may recover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clozapine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Infant 25% DEXTROSE Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: human hair found within an internal sample...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Jackson-Pratt Silicone Flat Drain Recalled by Cardinal Health 200, LLC Due...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Silicone Round Drain Recalled by Cardinal Health 200, LLC Due...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Silicone Round Drain Recalled by Cardinal Health 200, LLC Due...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Silicone Flat Drain Recalled by Cardinal Health 200, LLC Due...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE CONNECTOR 5 IN 1 20/BX Recalled by Teleflex Medical Due to Labeling: The...
The Issue: Labeling: The expiration date is not stated on the labeling, there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Silicone Round Drain Recalled by Cardinal Health 200, LLC Due...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...
The Issue: Product's seal possibly compromised, potentially compromising the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE CONNECTOR 3/8 Y 20/BX Recalled by Teleflex Medical Due to Labeling: The...
The Issue: Labeling: The expiration date is not stated on the labeling, there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.