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. 2,373 recalls have been distributed to South Dakota in the last 12 months.
Showing 22221–22240 of 47,632 recalls
Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...
The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...
The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spine & Trauma 3D Navigation 1.0 (subpart of the system Recalled by Brainlab...
The Issue: In certain occurrences, the affected navigation software application might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity i Processing Module LN 03R65-01 - Product Usage: Recalled by...
The Issue: The safety interlock covering the septum piercing probes within the bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM Recalled by Biomet 3i, LLC Due to...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM Recalled by Biomet 3i, LLC Due to...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity c Processing Module LN 03R67-01 - Product Usage: Recalled by...
The Issue: The safety interlock covering the septum piercing probes within the bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moxifloxacin Ophthalmic Solution USP Recalled by Lupin Pharmaceuticals Inc....
The Issue: Failed Impurities/Degradation Specifications: Expansion of July 2018 and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Telmisartan and Hyrdochlorothiazide Tablets Recalled by Macleods Pharma Usa...
The Issue: Failed Content Uniformity Specifications: The product is out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Telmisartan and Hyrdochlorothiazide Tablets 80 mg/25 mg Recalled by Macleods...
The Issue: Failed Content Uniformity Specifications: The product is out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Telmisartan and Hyrdochlorothiazide Tablets 40mg/12.5 mg Recalled by...
The Issue: Failed Content Uniformity Specifications: The product is out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach...
The Issue: Updates to the Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.