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. 2,295 recalls have been distributed to South Dakota in the last 12 months.
Showing 40501–40520 of 47,632 recalls
Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...
The Issue: A stock check revealed broken glass fibers between the connector and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ Percutaneous Sheath Introducer Kits The Percutaneous sheath...
The Issue: Arrow is recalling the Arrow¿ Percutaneous Sheath Introducer Kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...
The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TX1 Tissue Removal System. TX1 Procedure Pack P/N 554-1003-001 (outer box)...
The Issue: The sterile barrier in the packaging may be compromised due to cracks in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Laureate 0.035" (0.89mm) Hydrophilic Guide Wire Recalled by Merit...
The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Laureate Hydrophilic Guide Wire Recalled by Merit Medical Systems,...
The Issue: Discrepancy between the carton and unit labeling for the Merit Laureate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength Recalled by...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Jolly Time Microwave popcorn Recalled by American Pop Corn Co Due to The...
The Issue: The product has the potential to be contaminated with stainless steel metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jolly Time Microwave popcorn Recalled by American Pop Corn Co Due to The...
The Issue: The product has the potential to be contaminated with stainless steel metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jolly Time Microwave popcorn Recalled by American Pop Corn Co Due to The...
The Issue: The product has the potential to be contaminated with stainless steel metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sodium Chloride Hypertonicity Ophthalmic Ointment Recalled by Bausch & Lomb,...
The Issue: Crystallization: Crystal precipitate formation and an increase in the number...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Muro 128 (sodium chloride) hypertonicity ophthalmic ointment Recalled by...
The Issue: Crystallization: Crystal precipitate formation and an increase in the number...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Wockhardt Usa Inc....
The Issue: Failed Dissolution Specifications: Failure of dissolution test observed at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pastene ITALIAN FARFALLE #66 Recalled by The Pastene Companies Ltd. Due to...
The Issue: Semolina pasta fails to declare the allergen"wheat"
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pastene ITALIAN PAPPARDELLE Recalled by The Pastene Companies Ltd. Due to...
The Issue: Semolina pasta fails to declare the allergen"wheat"
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pastene ITALIAN RIGATONI #31 Recalled by The Pastene Companies Ltd. Due to...
The Issue: Semolina pasta fails to declare the allergen"wheat"
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pastene ITAL LONG FUSILLI Recalled by The Pastene Companies Ltd. Due to...
The Issue: Semolina pasta fails to declare the allergen"wheat"
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pastene ITALIAN ZITI RIGATI #20 Recalled by The Pastene Companies Ltd. Due...
The Issue: Semolina pasta fails to declare the allergen"wheat"
Recommended Action: Do not consume. Return to store for a refund or discard.