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. 2,554 recalls have been distributed to South Dakota in the last 12 months.
Showing 3401–3420 of 47,632 recalls
Recalled Item: LithoCrushV Single Use Mechanical Lithotriptor V. Model Number:...
The Issue: Potential for distal tip tearing of the Mechanical Lithotriptor V.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1)...
The Issue: Complaints have been received regarding post-operative implant collapse.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clobazam Tablets Recalled by Amerisource Health Services LLC Due to Presence...
The Issue: Presence of Foreign Tablets/Capsules
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Premium Dressing Change Kit with Recalled...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: IMed Products Product Name: Dressing Change Kit with Recalled by...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Cloth Recalled...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Transparent...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Tacy Medical Recalled by Trinity Sterile, Inc. Due to Potential...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cucumbers Recalled by WHOLESALE PRODUCE SUPPLY LLC DBA Due to Potential...
The Issue: Cucumbers may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acetaminophen Recalled by Akron Pharma, Inc. Due to Labeling: Not Elsewhere...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine HCl 25 mg Recalled by Akron Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine HCl 50 mg Recalled by Akron Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Regular Strength Recalled by Akron Pharma, Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine HCl 25 mg Recalled by Akron Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Extra Strength 500 mg Recalled by Akron Pharma, Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Extra Strength 500 mg Recalled by Akron Pharma, Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nhan Sam Tuyet Lien Truy Phong Hoan Recalled by Buy-Herbal Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found the products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FORCE FOREVER 400mg Tablets Recalled by GNMart LLC Due to Marketed without...
The Issue: Marketed without an approved NDA/ANDA. FDA analysis found the product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dabigatran Etexilate Recalled by Ascend Laboratories, LLC Due to CGMP...
The Issue: CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dabigatran Etexilate Recalled by Ascend Laboratories, LLC Due to CGMP...
The Issue: CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.