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. 2,442 recalls have been distributed to South Dakota in the last 12 months.
Showing 18321–18340 of 27,558 recalls
Recalled Item: Maintenance Kit PH2 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/ IMMULITE 1000 Progesterone Recalled by Siemens Healthcare...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Kit PH1 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75...
The Issue: Endologix updated information on the rates of Type III endoleaks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX2 Endovascular AAA System Item No. Item Description F00820-01...
The Issue: Endologix updated information on the rates of Type III endoleaks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Total Knee System Vanguard Open Box Femoral Components Item...
The Issue: packaging of some femoral components was incorrectly labeled as either...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUINTUBE Monitor Pack (5 tubes/pk Recalled by Stryker Leibinger GmbH & Co....
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceftriaxone TX 32 US S30 Recalled by BioMerieux SA Due to Potential...
The Issue: Potential performance issue on strain categorization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion Pump Recalled by Hospira Inc., A Pfizer Company Due to...
The Issue: Depleted Battery alarm shows instead of Replace Battery. On battery power,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Radial Head Prosthesis System Recalled by Synthes (USA) Products LLC...
The Issue: There is the possibility that the radial stem may loosen post-operatively at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-112: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-120: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-130: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-115: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-110: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.