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. 1,060 recalls have been distributed to South Dakota in the last 12 months.
Showing 9061–9080 of 27,558 recalls
Recalled Item: REGARD Newborn Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Basic Cataract tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PUMP SET Recalled by B. Braun Medical, Inc. Due to Leakage of the pump set...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Pump Measured Volume Solution Set/ w/ Auto Shut-Off. Single-use...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Pump Primary Administration Set w/ micro Tubing for Epidural...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Aire-Cuf Endotracheal Tube Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Uncuffed Wire Endotracheal Tubes Recalled by Smiths Medical ASD Inc....
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access hsTnI High Sensitivity Troponin I Recalled by Beckman Coulter Inc....
The Issue: Through customer feedback, testing a sample with cardiac troponin I...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Manifolds. (1) NAMIC Angiographic MANIFOLD Recalled by Medline...
The Issue: Potential for sterile barrier breach. Microscopic pinholes within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll (SL-2593CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.