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. 1,191 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,191 in last 12 months

Showing 2281–2300 of 51,434 recalls

Medical DeviceJune 4, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 M20. Fluoroscopic X-Ray System. Recalled by PHILIPS MEDICAL...

The Issue: Potential for bolts connecting the gearbox to the mounting flange of the...

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

Class II — Potential Health HazardOngoing
FoodJune 4, 2025· Bornstein Seafoods Inc

Recalled Item: Bornstein Frozen Shrimp Meat Recalled by Bornstein Seafoods Inc Due to...

The Issue: The recall was the result of the firm's routine sampling program and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 4, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA¿ 120/2120/2120i SETpoint Calibrator Recalled by Siemens Healthcare...

The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2025· C.R. Bard Inc

Recalled Item: BD Heyman Follower Coude Tip for following sizes: 12Fr - Recalled by C.R....

The Issue: Cather packaging may contain the incorrect French size.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2025· Hamilton Medical AG

Recalled Item: Hamilton C6 (ESM Board PN 10144626 UDI-DI code: Recalled by Hamilton Medical...

The Issue: A mechanical defect on a printed circuit board (PCB) as a result of PCB...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2025· C.R. Bard Inc

Recalled Item: Recalled by C.R. Bard Inc Due to Cather packaging may contain the incorrect...

The Issue: Cather packaging may contain the incorrect French size.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2025· ICU Medical, Inc.

Recalled Item: SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve Recalled by...

The Issue: Due to a manufacturing issue, disinfecting cap for needle-free connectors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2025· Given Imaging Ltd.

Recalled Item: Bravo CF capsule delivery device Recalled by Given Imaging Ltd. Due to It...

The Issue: It has been determined that misapplied adhesive on the Bravo CF capsule...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2025· C.R. Bard Inc

Recalled Item: BD Heyman Follower Straight Tip for following sizes: 10Fr - Recalled by C.R....

The Issue: Cather packaging may contain the incorrect French size.

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

Class II — Potential Health HazardOngoing
FoodJune 3, 2025· Peak Cocktails

Recalled Item: Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans Recalled by Peak...

The Issue: Overpressurization leading to exploding cans

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 2, 2025· Medshape, INC.

Recalled Item: Medshape Universal Joints Recalled by Medshape, INC. Due to Bone external...

The Issue: Bone external fixation system may have the pin that can become dislodged...

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

Class II — Potential Health HazardOngoing
DrugJune 2, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Amneal...

The Issue: Microbial contamination of non-sterile products: tablets may exhibit black...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: LIDOcaine HCL Sterile Injection Recalled by Tailstorm Health INC Due to Lack...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: LIDOcaine HCl Injection Recalled by Tailstorm Health INC Due to Lack of...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: BUPIVAcaine HCL Sterile injection Recalled by Tailstorm Health INC Due to...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: KETAmine Hydrochloride Injection Recalled by Tailstorm Health INC Due to...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: LIDOcaine HCL Sterile Injection Recalled by Tailstorm Health INC Due to Lack...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: KETAmine Hydrochloride Injection Recalled by Tailstorm Health INC Due to...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 30, 2025· Remote Diagnostic Technologies Ltd.

Recalled Item: Inseego USB8 4G Dongle Kit Recalled by Remote Diagnostic Technologies Ltd....

The Issue: Kit USB flash drive contains outdated software, which could result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2025· Maquet Critical Care AB

Recalled Item: Servo-n Ventilator System. Model Number: 6694800. Recalled by Maquet...

The Issue: Potential for inaccurate measurement of the patient circuit compliance...

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

Class I — Serious Health HazardOngoing