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. 2,360 recalls have been distributed to South Dakota in the last 12 months.
Showing 26261–26280 of 27,558 recalls
Recalled Item: BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators are...
The Issue: The BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brookstone Heated Body Bean Recalled by Brookstone Company, Inc. Due to...
The Issue: Additional Warning Statement to prevent burns to the skin
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS Reamer Sleeve KNEE REAMER SLEEVE 13.0 thru 20.0 Recalled by Biomet, Inc....
The Issue: Biomet has initiated this action following an investigation which identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Immunodiagnostic Products Anti-HBs (total antibody to hepatitis B...
The Issue: Ortho Clinical Diagnostics is recalling certain lots of the Vitros Anti-HBs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to It has...
The Issue: It has been determined that, in some cases, pulley drive components have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Modular Humeral Head 48mm x 24mm Ti 6AI4V/Ion Implanted (Orthopedic...
The Issue: The items in this lot are missing the ion implantation feature. The surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Operations,...
The Issue: On cobas c 701 and cobas c 702 modules of the Cobas 8000 series analyzer, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS Reamer Sleeve KNEE REAMER SLEEVE 8.0 THRU 12.5 Recalled by Biomet, Inc....
The Issue: Biomet has initiated this action following an investigation which identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADstream software. Product Usage: CADstream is an image processing system...
The Issue: An incorrect biopsy or missed target could result if the incorrect grid is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical RUMI Arch Recalled by Cooper Surgical, Inc. Due to Excessive...
The Issue: Excessive pressure exerted on the uterine tip when attached to the Arch may,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Advincula Arch Recalled by Cooper Surgical, Inc. Due to...
The Issue: Excessive pressure exerted on the uterine tip when attached to the Arch may,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Overhead Rail System Recalled by Hill-Rom, Inc. Due to Liko/Hill-Rom to...
The Issue: Liko/Hill-Rom to date has received two reports from facilities alleging that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.