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. 2,447 recalls have been distributed to South Dakota in the last 12 months.
Showing 17861–17880 of 27,558 recalls
Recalled Item: PARADYM Models: VR 8250 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTENSIA Models: VR 124 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OVATIO Models: VR 6250 Recalled by Sorin Group Italia SRL - CRF Due to Sorin...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoGuard Closed Luer Connector Recalled by B Braun Medical Inc Due to B....
The Issue: B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys PreciControl Varia 3 Recalled by Roche Diagnostics Corporation Due...
The Issue: e-barcode and value sheet for PreciControl Varia contains a typographical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional...
The Issue: Potential Patient Demographic Error with Blank Patient ID Field
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit...
The Issue: The current secondary packaging, a box, incorrectly states that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eMAG System Recalled by bioMerieux, Inc. Due to Some anomalies have been...
The Issue: Some anomalies have been identified during manufacturing controls.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite...
The Issue: Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for Recalled...
The Issue: Complaints concerning kinked haptics that were occurring during lens delivery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mederi Stretta Catheter and Accessory Kit Recalled by Mederi Therapeutics,...
The Issue: Product sterility compromised due to breach in sterile barrier package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between...
The Issue: The second generation neoBLUE 2 lights with a black band, sold from 2003 to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter has confirmed that the Export feature located in the Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun 5000 Temperature Management System Recalled by C.R. Bard, Inc....
The Issue: Potential failure of the Arctic Sun 5000 Temperature Management System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optional MDRC-1119 Front Cover Attachment Kit for review display monitors....
The Issue: If metal strips are removed and re-applied to another display, there is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Back Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Knee/Shldr Recalled by Breg Inc Due to They may not have been...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Shldr XL Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.