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. 2,311 recalls have been distributed to South Dakota in the last 12 months.
Showing 39701–39720 of 47,632 recalls
Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excella II Standard Pedicle Screw Recalled by Innovasis, Inc Due to Mislabeling
The Issue: Innovasis is recalling the Excella II Standard Pedicle Screw due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Succinate Extended-release Tablets Recalled by Mylan...
The Issue: Presence of Foreign Tablets/Capsules: A pharmacist reported a rogue tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....
The Issue: Failed PH Specifications: It has been determined that the pH of the lots...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....
The Issue: Failed PH Specifications: It has been determined that the pH of the lots...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UltraBalance Protein Powder Recalled by Metagenics, Inc. Due to Undeclared Soy
The Issue: Metagenics is recalling UltraBalance Protein powder because it may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...
The Issue: In specific situation a partially truncated file may be written to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z-HD (barium sulfate) For Suspension (98% w/w) Recalled by Bracco...
The Issue: Subpotent Drug: Low out of specification results for both pH and assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...
The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL Recalled by Smith & Nephew, Inc....
The Issue: There was an error in manufacturing which resulted in the proximal lag screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.