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 27421–27440 of 27,558 recalls
Recalled Item: 00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789504001 VerSys Femoral Head Provisional 40mm -3.5 00789504002 VerSys...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 100789502202 VerSys Femoral Head Provisional 22mm +0 00789502203...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: . 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789503201 VerSys Femoral Head Provisional 32mm -3.5 00789503202 VerSys...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: . 00789503601 VerSys Femoral Head Provisional 36mm -3.5 00789503602 VerSys...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Laboratory LabAccess Results Workstation (LARS) Recalled by...
The Issue: The recall was initiated because Sunquest has confirmed that the Sunquest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0...
The Issue: In January 2010, Medtronic issued a recall of Medtronic NIM 3.0 Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0...
The Issue: In January 2010, Medtronic issued a recall of Medtronic NIM 3.0 Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0...
The Issue: In January 2010, Medtronic issued a recall of Medtronic NIM 3.0 Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Electrolyte reagent (for Synchron LX Systems and UniCel Recalled by...
The Issue: Beckman Coulter is recalling the Synchron Systems LX20/UniCel DxC ISE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kimberly-Clark Patient Warming System - Model 1000 Control Unit The Recalled...
The Issue: Error 85 alarm on the Model 1000 Control Unit was occasionally triggered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 HPLC. Used as an aid in the detection and Recalled by Tosoh Bioscience...
The Issue: The Beta-thalessemia Mode of the G7 Analyzer-Beta Thalassemia Mode is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM 6/7 Patient Monitor Manufactured in China for : Mindray DS USA Recalled...
The Issue: There is an issue with the DPM 6 and DPM 7 monitors where the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polar Dressing Recalled by Breg Inc, An Orthofix Company Due to Mislabeling
The Issue: This recall has been initiated due to confirmation that the Polar Dressing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boule Con-Diff Hematology Control 9 vials. For in vitro diagnostic Recalled...
The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled the Boule Con...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.