Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 983 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
983 in last 12 months

Showing 25221–25240 of 48,215 recalls

Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 460 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 360 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 280 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 320 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 440 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 280 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 440 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 360 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 13 mm x 280 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 360 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 11 mm x 420 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 260 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 320 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: RAPIDLab 1245 Blood Gas Analyzer Recalled by Siemens Healthcare Diagnostics,...

The Issue: Therapeutic levels (1mg/mL and 2mg/mL) of Hydroxocobalamin may interfere...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F010 Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: AIIuraXperFDlO/10 Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD2O Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· In2bones USA, LLC

Recalled Item: CoLink(TM) Lapidus Plate XP Recalled by In2bones USA, LLC Due to CoLink(TM)...

The Issue: CoLink(TM) Lapidus Plate +2mm Right and Left, were laser marked incorrectly....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD2O Biplane Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: AIIuraXperFDlO Recalled by Philips Electronics North America Corporation Due...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing