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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 27161–27180 of 47,632 recalls
Recalled Item: Concorde Lift Driver Shaft AO. Used with supplemental internal spinal...
The Issue: Potential for Intra-operative breakage of driver tips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Titanium Calibrated Reaming Rod Recalled by Synthes (USA) Products...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Guide Rod Recalled by Synthes (USA) Products LLC Due to Possible lack...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARROW PICC powered by ARROW VPS Stylet Recalled by Arrow International Inc...
The Issue: Finished good kits may contain incorrect components. Kits that should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ArrowADVANTAGE 5 Pressure Injectable Peripherally Inserted Central Catheter...
The Issue: Finished good kits may contain incorrect components. Kits that should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Imaging version V31 (model # 10014063) is a Picture Recalled by...
The Issue: Siemens is releasing a letter to inform about potential data loss relevant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LaBri's Body Health XPLODE 30 capsules Exclusively distribute worldwide by...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Famotidine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Tablet/Capsule Specification; out of specification for tablet weight
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Platinium VR DF4 1240 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium CRT-D 1741 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium DR DF4 1540 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium VR 1210 Recalled by Sorin Group Italia SRL - CRF Due to There is a...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium CRT DF1 1711 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium DR 1510 Recalled by Sorin Group Italia SRL - CRF Due to There is a...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew POLARSTEM(TM) Femoral Stems with Ti/HA (Standard Recalled by...
The Issue: The Cardan joint of the Polarstem Cardan could potentially fracture or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.