Product Recalls in Colorado

Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,728 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,728 in last 12 months

Showing 421440 of 51,434 recalls

Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000F Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000H Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000V Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000C Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical, Inc.

Recalled Item: Tego Connector: Recalled by ICU Medical, Inc. Due to Needle free access...

The Issue: Needle free access device intended as accessory to vascular access used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Tyber Medical

Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...

The Issue: The supplier manufactured anatomical left plates with an incorrect thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Tyber Medical

Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...

The Issue: The supplier manufactured anatomical left plates with an incorrect thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: VANTAGE GALAN 3T Model MRT-3020/MEXL-3020 Recalled by Canon Medical System,...

The Issue: There is a potential for formation of ice occurring in the venting system of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical Inc.

Recalled Item: Pulsator Arterial Blood Sampling Kit Recalled by ICU Medical Inc. Due to...

The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: VANTAGE TITAN 3T Model MRT-3010/MEXL-3010 Recalled by Canon Medical System,...

The Issue: There is a potential for formation of ice occurring in the venting system of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical Inc.

Recalled Item: Portex Spinal Tray Recalled by ICU Medical Inc. Due to Affected lots of...

The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...

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

Class II — Potential Health HazardOngoing
FoodDecember 18, 2025· DIRECT SOURCE SEAFOOD LLC

Recalled Item: waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & Recalled by DIRECT...

The Issue: Shrimp may be contaminated with Cesium-137 (Cs-137).

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 18, 2025· DIRECT SOURCE SEAFOOD LLC

Recalled Item: MARKET 32 by Price Chopper brand Recalled by DIRECT SOURCE SEAFOOD LLC Due...

The Issue: Shrimp may be contaminated with Cesium-137 (Cs-137).

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2025· Imprimis NJOF, LLC

Recalled Item: Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL Recalled by Imprimis NJOF, LLC Due to...

The Issue: Presence of particulate matter - Glass like particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2025· Imprimis NJOF, LLC

Recalled Item: Dexamethasone Moxifloxacin Ketorolac Recalled by Imprimis NJOF, LLC Due to...

The Issue: Presence of particulate matter - Glass like particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2025· Imprimis NJOF, LLC

Recalled Item: Dexamethasone Moxifloxacin Recalled by Imprimis NJOF, LLC Due to Presence of...

The Issue: Presence of particulate matter - Glass like particles.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 18, 2025· Vascutek, Ltd.

Recalled Item: Gelsoft Plus Recalled by Vascutek, Ltd. Due to Gelatin sealed woven...

The Issue: Gelatin sealed woven polyester prostheses devices, designed for vascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Wilson-Cook Medical Inc.

Recalled Item: Teslatome Bipolar Sphincterotomes Model Number: G60784 UDI-DI code: Recalled...

The Issue: Due to product that may contain a void in the material that separates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing