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. 2,526 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,526 in last 12 months

Showing 1242112440 of 27,462 recalls

Medical DeviceNovember 21, 2019· Medtronic Inc.

Recalled Item: Medtronic MiniMed 670G System with SmartGuard Recalled by Medtronic Inc. Due...

The Issue: There have been reported incidents of a loose reservoir that can no longer...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 21, 2019· Caire, Inc.

Recalled Item: CAIRE MODEL: FreeStyle Comfort Oxygen Concentrator - Product Usage: The...

The Issue: Four units of European version FreeStyle Comfort were distributed in the US,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2019· Stryker GmbH

Recalled Item: Stryker Pin To Rod Coupling External Fixation System Hoffmann II Recalled by...

The Issue: Pin To Rod Coupling could not clamp the pin and rod as intended

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2019· STANLEY BLACK & DECKER INC.

Recalled Item: The products involved are DeWALT laser distance measurers Recalled by...

The Issue: The products are labeled as Class II lasers. However, the level of laser...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2019· 3M Company - Health Care Business

Recalled Item: 3M Durapore Advanced Recalled by 3M Company - Health Care Business Due to...

The Issue: While the product meets all safety and efficacy criteria, long term exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2019· DeRoyal Industries Inc

Recalled Item: DeRoyal KNEE BRACE Recalled by DeRoyal Industries Inc Due to The Warrior...

The Issue: The Warrior Recovery Knee Brace has the potential to come apart due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Outlook Safety Infusion System Y-type Blood Set Recalled by B. Braun...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry CardioPhase High Sensitivity C-Reactive Protein (hsCRP)...

The Issue: Atellica and ADVIA hsCRP calibrator accuracy has drifted away from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH High Sensitivity C-Reactive Protein (HsCRP) Calibrator - Product...

The Issue: Atellica CH: The Atellica¿ CH High Sensitivity CReactive Protein Calibrator...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Cardiac Assist, Inc

Recalled Item: TandemLife ECLS Procedure Kit - V24/A17 Recalled by Cardiac Assist, Inc Due...

The Issue: The kit contained a 29Fr ProtekDuo cannula instead of a 24Fr Protek Solo...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT Recalled by...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: MICRO-PSD HDR Recalled by Angiodynamics, Inc. Due to May result in readings...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: MICRO-PSD Electron Recalled by Angiodynamics, Inc. Due to May result in...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing