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. 980 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
980 in last 12 months

Showing 22901–22920 of 48,219 recalls

Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Bullet Tip...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Smooth Guide Wire - Bullet Tip Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Becton Dickinson & Co.

Recalled Item: BD BBL Trypticase Soy Agar with 5% Sheep Blood Recalled by Becton Dickinson...

The Issue: a portion of a single lot was not manufactured in accordance with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Smooth Recalled by...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Pressure Sentinel¿ Intramedullary Reaming System Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Humeral Guide Wire - Ball Tip Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS zee biplane systems with Material 10094141- a Angiographic x-ray...

The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Q.zen biplane with Material 10848355 - a Angiographic x-ray Recalled...

The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Q biplane with Material 10848282- - a Angiographic x-ray Recalled by...

The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...

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

Class II — Potential Health HazardOngoing
DrugOctober 19, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: Fentanyl (10 mcg/mL) in NS 1 mL (in 3mL BD Syringe) Recalled by Avella of...

The Issue: Lack of assurance of sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: Morphine (1 mg/mL) in NS 100 mL Bag Recalled by Avella of Deer Valley, Inc....

The Issue: Lack of assurance of sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2018· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's 24 Hour Allergy (cetirizine hydrochloride) Oral Solution 1 mg/mL...

The Issue: Failed Impurities/Degradation Specifications: unknown impurity higher than...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund