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. 2,163 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,163 in last 12 months

Showing 34013420 of 51,434 recalls

Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/20 System Code: (1) 722038 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026 Recalled by PHILIPS...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 5 M12 System Code: (1) 722227 (2) 722231 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXperFD20/15 System Code: (1) 722058 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) Recalled by PHILIPS...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 3 M12 System Code: (1) 722063 (2) 722221 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXperFD20/10 System Code: (1) 722029 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
FoodJanuary 13, 2025· Monkey Spit

Recalled Item: Monkey Spit "Monkey Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...

The Issue: Barbeque sauce product contains undeclared listing of (Milk) in product...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 13, 2025· Monkey Spit

Recalled Item: Monkey Spit "Atomic Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...

The Issue: Barbeque sauce product contains undeclared allergen listing of (Milk) in...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 13, 2025· Monkey Spit

Recalled Item: Monkey Spit "Swamp Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...

The Issue: Barbeque sauce product contains undeclared allergens (soy) contained in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 13, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by The Harvard Drug Group...

The Issue: CGMP Deviations: presence of Nitrosamine Drug Substances Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL Recalled by Teva...

The Issue: Failed Stability Specifications - 12-month stability test result for one of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 10, 2025· Spectranetics Corporation

Recalled Item: Intact Vascular Tack Endovascular System Recalled by Spectranetics...

The Issue: Use of Tack Endovascular system, designed to treat acute dissections of...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2025· Integra LifeSciences Corp.

Recalled Item: Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Recalled by...

The Issue: Potential that the induction seal is not completely sealed to the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis: MedFlex Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing device labeling is being updated to strengthen labeling...

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

Class II — Potential Health HazardOngoing