Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,285 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,285 in last 12 months

Showing 401420 of 27,462 recalls

Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2025· HANGZHOU BEVER MEDICAL DEVICES CO., LTD.

Recalled Item: BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip Recalled by...

The Issue: Labeling error, Incorrect expiration date

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2025· Baxter Healthcare Corporation

Recalled Item: SIGMA Spectrum Infusion Pump Recalled by Baxter Healthcare Corporation Due...

The Issue: Certain pumps have potentially been released from service with defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Remote Diagnostic Technologies Ltd.

Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...

The Issue: Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing