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. 2,723 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,723 in last 12 months

Showing 27612780 of 51,434 recalls

Medical DeviceMarch 24, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn CONNEX Accessory Power Management Stand: Recalled by Baxter...

The Issue: There were customer reports of devices which experienced battery-related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Boston Scientific Corporation

Recalled Item: IceSeed 1.5 CX NEEDLE US Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 0.5T Standard Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits Recalled by...

The Issue: A single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: SmartPath to dStream for 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Power/Pulsar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: SmartPath to dStream for 3.0T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T R11 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Explorer/Nova Dual Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 650C A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 750c A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 620 A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 650 A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 650C A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 620 SE Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 650c A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing