Product Recalls in Oklahoma

Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,496 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,496 in last 12 months

Showing 2104121060 of 28,654 recalls

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 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 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 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 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 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 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 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 39 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 57 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 11 consists of all product under product code JDI 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 33 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 38 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 58 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 55 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 6 consists of all products 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 2 consists of all products product code LPH 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 61 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 68 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 21 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