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. 2,452 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,452 in last 12 months

Showing 1588115900 of 27,558 recalls

Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire Bullet Tip 3.0 mm Diameter...

The Issue: Potential failure of sterile packaging seal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: 708033 URODiagnost As a multifunctional universal imaging application system...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Smooth Guide Wire Bullet Tip 3.0 mm Diameter Recalled by Zimmer Biomet, Inc....

The Issue: Potential failure of sterile packaging seal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Pressure Sentinel Intramedullary Reaming System Guide Wire Bullet Tip 2.4...

The Issue: Potential failure of sterile packaging seal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Beckman Coulter Inc.

Recalled Item: BECKMAN COULTER MicroScan MICroSTREP Plus Panel Recalled by Beckman Coulter...

The Issue: Beckman Coulter has received customer complaints of lowered minimum...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: Mutlidiagnost-Eleva with Flat Detector Eleva with Flat Detector 708037 As...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: MultiDiagnostic-Eleva with Flat Detector 708035 As a multifunctional...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Tornier, Inc

Recalled Item: AEQUALIS HUMERAL NAIL DRILL BIT Recalled by Tornier, Inc Due to Drill bit...

The Issue: Drill bit tips without new BargerGard tip protector may puncture through...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: MultiDiagnost Eleva 708036 As a multifunctional universal imaging...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Recalled by...

The Issue: Potential failure of sterile packaging seal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: MultiDiagnostic-Eleva with Flat Detector 708038 As a multifunctional...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: Mutlidiagnost-Eleva with Flat Detector 708034 As a multifunctional universal...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing