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. 2,596 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,596 in last 12 months

Showing 1720117220 of 51,434 recalls

DrugDecember 9, 2020· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Hydroxyzine Hydrochloride Oral Solution Recalled by Morton Grove...

The Issue: Failed Impurities/Degradation Specification: OOS for the following - unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 9, 2020· Biogen MA Inc.

Recalled Item: Vumerity (diroximel fumarate) delayed-release capsule Recalled by Biogen MA...

The Issue: Failed dissolution specifications: out-of-specification test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 9, 2020· Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Docetaxel Injection USP 160 mg/8mL (20 mg/mL) Recalled by Shilpa Medicare...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Busulfan Injection 60 mg/10 mL (6 mg/mL) Recalled by Shilpa Medicare Limited...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Azacitidine for Injection 100 mg/vial Recalled by Shilpa Medicare Limited...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Azacitidine for Injection 100 mg/vial Recalled by Shilpa Medicare Limited...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Imatinib Mesylate Tablets 400 mg Recalled by Shilpa Medicare Limited Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Imatinib Mesylate Tablets 100 mg Recalled by Shilpa Medicare Limited Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 8, 2020· Canon Medical System, USA, INC.

Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000C Catheterization...

The Issue: System table may tilt because the bolts that fasten the vertical column and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Canon Medical System, USA, INC.

Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization...

The Issue: System table may tilt because the bolts that fasten the vertical column and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Canon Medical System, USA, INC.

Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000F Catheterization...

The Issue: System table may tilt because the bolts that fasten the vertical column and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Medtronic Neurosurgery

Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...

The Issue: There is a potential for a defect on the seal of the outer pouch of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Becton Dickinson & Co.

Recalled Item: BD Phoenix PMIC-107: IVD is intended for the in vitro Recalled by Becton...

The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· PHILIPS HOME HEALTHCARE SOLUTION

Recalled Item: ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system Recalled by...

The Issue: After the user selects the Lock-in command, the kV and mA values are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Becton Dickinson & Co.

Recalled Item: BD Phoenix PMIC/ID-108: IVD is intended for the in vitro Recalled by Becton...

The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Becton Dickinson & Co.

Recalled Item: BD Phoenix PMIC-108: IVD is intended for the in vitro Recalled by Becton...

The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Roche cobas 8000 modular analyzer series (i.e. Recalled by Roche Diagnostics...

The Issue: Potential for Changed Configuration Settings on the cobas 8000 modular...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Becton Dickinson & Co.

Recalled Item: BD Phoenix PMIC-110: IVD is intended for the in vitro Recalled by Becton...

The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Becton Dickinson & Co.

Recalled Item: BD Phoenix" PMIC-109: IVD is intended for the in vitro Recalled by Becton...

The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...

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

Class II — Potential Health HazardOngoing