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. 2,573 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,573 in last 12 months

Showing 961980 of 48,219 recalls

Medical DeviceOctober 20, 2025· Medtronic Perfusion Systems

Recalled Item: Medtronic HR-ACT (High Range Activated Clotting Time Cartridges) Recalled by...

The Issue: Medtronic personnel observed trace amounts of dry blood on the external...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2025· Auris Health, Inc

Recalled Item: MONARCH Bronchoscope. Model Number: MBR-000211-B Recalled by Auris Health,...

The Issue: Potential that product was leak tested with equipment outside of its...

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

Class II — Potential Health HazardOngoing
DrugOctober 17, 2025· Aero Healthcare

Recalled Item: Acetaminophen 500mg Caffeine 65mg caplets Recalled by Aero Healthcare Due to...

The Issue: Labeling: Label Mix-up. This issue affects the outer box labeling only. The...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 17, 2025· Straumann USA LLC

Recalled Item: Emdogain Recalled by Straumann USA LLC Due to The possibility for this...

The Issue: The possibility for this product that is intended for demonstration purposes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· INTELERAD MEDICAL SYSTEMS INCORPORATED

Recalled Item: IntelePACS - InteleConnect / TechPortal Recalled by INTELERAD MEDICAL...

The Issue: Software application that receives digital images and data to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris infusion Pump Module 8100 Recalled by CareFusion 303, Inc. Due to...

The Issue: If infusion pump is dropped or severely jarred this may damage the pump...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2025· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an Recalled...

The Issue: Potential of negative recovery of the HBsAg analyte across two (2) lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem ID-B. Model Number: SR103B. Intended for use as an Recalled by...

The Issue: Potential of negative recovery of the HBsAg analyte across two (2) lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
FoodOctober 16, 2025· M.C.I. Foods, Inc.

Recalled Item: Egg and Cheese Breakfast Burrito Recalled by M.C.I. Foods, Inc. Due to...

The Issue: Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 16, 2025· M.C.I. Foods, Inc.

Recalled Item: Cheese and Egg with Green Salsa Breakfast Burrito Recalled by M.C.I. Foods,...

The Issue: Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 16, 2025· Amerisource Health Services LLC

Recalled Item: Prazosin Hydrochloride Recalled by Amerisource Health Services LLC Due to...

The Issue: Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2025· Amerisource Health Services LLC

Recalled Item: Prazosin Hydrochloride Recalled by Amerisource Health Services LLC Due to...

The Issue: Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2025· Amerisource Health Services LLC

Recalled Item: Prazosin Hydrochloride Recalled by Amerisource Health Services LLC Due to...

The Issue: Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 16, 2025· SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION

Recalled Item: Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed...

The Issue: Due to an issue (potential breakage) with the shaft for the mounting of the...

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

Class II — Potential Health HazardOngoing