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 27141–27160 of 47,632 recalls
Recalled Item: iVue with Normative Database Recalled by Optovue, Inc. Due to FDA determined...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue 500 with iScan Recalled by Optovue, Inc. Due to FDA determined that a...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iFusion Recalled by Optovue, Inc. Due to FDA determined that a 510(k) is...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 2200TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559...
The Issue: The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for...
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: Concorde Lift Torque Limiting Handle. Must be used with supplemental...
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: Light Clip for Oracle Retractor Recalled by Synthes (USA) Products LLC Due...
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: 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: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Presence...
The Issue: Presence of Particulate Matter; stainless steel
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thymus Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: milk (Colostrum)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Liver-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: soy (lecithin)
Recommended Action: Do not consume. Return to store for a refund or discard.