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. 2,516 recalls have been distributed to South Dakota in the last 12 months.
Showing 7281–7300 of 47,632 recalls
Recalled Item: Achieva 1.5T Initial System Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Power/Pulsar Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips North America Llc Due to Potential component...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artri King con Origa y Omega 3 tablets Recalled by Botanical Be Due to...
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled by Glenmark...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Reumo Flex caplets Recalled by Botanical Be Due to Undeclared Diclofenac
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kuka Flex Forte caplets Recalled by Botanical Be Due to Undeclared Diclofenac
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Deferasirox Tablets for Oral Suspension Recalled by Glenmark Pharmaceuticals...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxaydo (oxycodone HCl Recalled by Zyla Life Sciences US Inc. Due to...
The Issue: Sub-potent Drug: Lower potency than labeled.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Opium Tincture Recalled by Edenbridge Pharmaceuticals, LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Item 19858 Recalled by GIVE AND GO PREPARED FOODS CORP Due to Potential...
The Issue: Potential plastic pieces in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Strong Iodine Solution U.S.P. (Lugol's Solution) (Iodine 5%) Recalled by...
The Issue: CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Processing Module The Alinity c Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.