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 2801–2820 of 47,632 recalls
Recalled Item: Medline Convenience kits used for various procedures: 1) PRECIP TRAY...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) DR. KHAN Recalled...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter NovumIQ Syringe INFUSION SYSTEM Recalled by Baxter Healthcare...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder Stem Recalled by ZIMMER ORTHOPEDICS MANFACTURING...
The Issue: Five complaints received where surgeon was unable to remove and/or connect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carvedilol Tablets USP 25 mg Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets USP 12.5 mg Recalled by Glenmark Pharmaceuticals Inc.,...
The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets USP 3.125mg Tablets a.)100-count bottle (NDC...
The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets USP 6.25 mg Recalled by Glenmark Pharmaceuticals Inc.,...
The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Walgreens Recalled by Sigan Industries Group Inc. Due to Chemical...
The Issue: Chemical Contamination: Presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phoroptor VRx Digital System Model Numbers: 16241 Recalled by Reichert, Inc....
The Issue: The head of the phoropter head could come loose and potentially detach due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoroptor VRx Digital System Model Numbers: 16242 Recalled by Reichert, Inc....
The Issue: The head of the phoropter head could come loose and potentially detach due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...
The Issue: Stability data does not support expiry: the products have the potential to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...
The Issue: Stability data does not support expiry: the products have the potential to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Premier Solo Diamond - Large Invented Cone Recalled by Premier Dental...
The Issue: The hardness not meeting the material specification and may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LPS Flex Recalled by Zimmer, Inc. Due to The "Use with plate 7, 8, 9,...
The Issue: The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration...
The Issue: Aspiration catheter distal tip features and characteristics may not be in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...
The Issue: Beckman Coulter has determined that device software versions V1.3, V1.4,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.