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. 2,396 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,396 in last 12 months

Showing 2026120280 of 27,558 recalls

Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 15 consists of all product code JDI Recalled by Zimmer Manufacturing...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 50 consists of all product under product code: JWH Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 24 consists of all product under product code: HRS Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 9 consists of all product under HRS Recalled by Zimmer Manufacturing...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 32 consists of all product under product code: HWC Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 41 consists of all product under product code: KTT Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 26 consists of all product under product code: JWH Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 49 consists of all product under product code: JWH Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 47 consists of all product under product code: LPH Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 40 consists of all product under product code: HSB Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 71 consists of all product under product code: JDI Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 13 consists of all product under product code HWC Recalled by Zimmer...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 22 consists of all product under product code: JDI Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 56 consists of all product under product code: HWC Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 72 consists of all product code: JDI and same Recalled by Zimmer...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 20 consists of all prod oct under poduct code: Recalled by Zimmer...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 42 consists of all product under product code: HSB Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 66 consists of all product under product code: JDI Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 70 consists of all product under product code: JDI Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Manufacturing B.V.

Recalled Item: Product 63 consists of all product under product code: LPH Recalled by...

The Issue: As a result of the insufficient sealer calibration data for product packaged...

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

Class II — Potential Health HazardOngoing