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 1221–1240 of 51,434 recalls

Medical DeviceSeptember 30, 2025· Medline Industries, LP

Recalled Item: MEDLINE convenience kits labeled as: GP-LEEP PACK-LF Recalled by Medline...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· IMPRIS Imaging Inc

Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...

The Issue: There is a potential safety issue associated with the magnet venting paths...

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

Class I — Serious Health HazardOngoing
DrugSeptember 29, 2025· Medline Industries, LP

Recalled Item: Medline Recalled by Medline Industries, LP Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acuity Specialty Products, Inc.

Recalled Item: AFCO Recalled by Acuity Specialty Products, Inc. Due to cGMP deviations: The...

The Issue: cGMP deviations: The recall was initiated because required receipt testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acella Pharmaceuticals, LLC

Recalled Item: Doxycycline Hyclate Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Failed dissolution specifications: Stability testing found that the lot did...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acuity Specialty Products, Inc.

Recalled Item: Wyandotte Recalled by Acuity Specialty Products, Inc. Due to cGMP...

The Issue: cGMP deviations: The recall was initiated because required receipt testing...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Gluteal Implant Product Name: Gluteal Implant Model/Catalog...

The Issue: Due to manufactured products that deviated from established specifications...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Pectoral Implant Product Name: Pectoral Implant...

The Issue: Due to manufactured products that deviated from established specifications...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Magnetic Rings for SAFE-T-FILL Blood Gas Capillaries Recalled by...

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: B105P Recalled by GE Healthcare Finland Oy Due to Potential loss of...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: Carescape B450 Recalled by GE Healthcare Finland Oy Due to Potential loss of...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog...

The Issue: Due to manufactured products that deviated from established specifications...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog...

The Issue: Due to manufactured products that deviated from established specifications...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog...

The Issue: Due to manufactured products that deviated from established specifications...

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

Class II — Potential Health HazardOngoing