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. 2,266 recalls have been distributed to South Dakota in the last 12 months.
Showing 43821–43840 of 47,632 recalls
Recalled Item: MINUTE MAID STRAWBERRY PASSION Flavored Juice Beverage Recalled by Coca-Cola...
The Issue: Products with the specific Lot Code and Codes listed above are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MINUTE MAID APPLE JUICE Recalled by Coca-Cola USA, Inc. Due to Products with...
The Issue: Products with the specific Lot Code and Codes listed above are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MINUTE MAID CRANBERRY APPLE RASPBERRY Flavored Juice Beverage Recalled by...
The Issue: Products with the specific Lot Code and Codes listed above are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MINUTE MAID ORANGE JUICE Recalled by Coca-Cola USA, Inc. Due to Products...
The Issue: Products with the specific Lot Code and Codes listed above are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MINUTE MAID Mixed Berry Juice Recalled by Coca-Cola USA, Inc. Due to...
The Issue: Products with the specific Lot Code and Codes listed above are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for Recalled by...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Elekta digital accelerators with electrons and beam modulator Recalled...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polarizer D Fixed w/Rotating Red 1 lambda plate. Utilized in Recalled by...
The Issue: Carl Zeiss Microscopy, LLC is recalling the Polarizer D component used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alair Bronchial Thermoplasty Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific has discovered an inconsistent "Use By" expiration date on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RigiflexTM 11 Single-Use Achalasia Balloon Dilator Recalled by Boston...
The Issue: Product labeled with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NephroMax high Pressure nephrostomy Balloon Catheter Kit. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NephroMax high Pressure Nephrostomy Balloon Catheter. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite Recalled...
The Issue: DJO, LLC has recently identified a product safety issue with the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON System(s) Lactate (LACT) Reagent. Product Usage: Lactate (LACT)...
The Issue: Beckman Coulter has confirmed customer reports of LACT Lot M210077 failing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.