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. 1,660 recalls have been distributed to South Dakota in the last 12 months.
Showing 46381–46400 of 47,632 recalls
Recalled Item: Thyro-Tab 0.300 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.050 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.125 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.112 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.137 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NAPROXEN TABLETS USP Recalled by Glenmark Generics Inc., USA Due to...
The Issue: Labeling: Label Mix-Up: Bottles labeled as Naproxen Tablets USP, 500 mg,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROCORTISONE and ACETIC ACID OTIC SOLUTION Recalled by Vintage...
The Issue: Impurities/Degradation Products: Out of specificiation results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROXYZINE HYDROCHLORIDE ORAL SOLUTION Recalled by Vintage Pharmaceuticals...
The Issue: Impurities/Degradation Products: High Out of Specification results for a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Unicel Closed Tube Aliquotter (UCTA) for UniCel DxC 660i Recalled by Beckman...
The Issue: The recall was initiated because Beckman Coulter has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extraneal and/or DIANEAL LOW CALCIUM Peritoneal Dialysis Solution in Plastic...
The Issue: Baxter discovered that a Baxter technical service representative was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finapres Medical Systems Portapres with NiMh battery pack Product Usage:...
The Issue: Battery may become hot and leak
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chocolate Peanut Butter Recalled by Arctic Zero, Inc. Due to Undeclared Milk
The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Coffee Recalled by Arctic Zero, Inc. Due to Undeclared Milk
The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate Recalled by Arctic Zero, Inc. Due to Undeclared Milk
The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate Dipped Bars Recalled by Arctic Zero, Inc. Due to Undeclared Milk
The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Strawberry Recalled by Arctic Zero, Inc. Due to Undeclared Milk
The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...
Recommended Action: Do not consume. Return to store for a refund or discard.