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. 1,065 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,065 in last 12 months

Showing 19341–19360 of 51,434 recalls

DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Simvastatin Tablets Recalled by Aurobindo Pharma USA Inc. Due to CGMP...

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Mirtazapine Tablets Recalled by Aurobindo Pharma USA Inc. Due to CGMP...

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Oxycodone and Acetaminophen Tablets Recalled by Aurobindo Pharma USA Inc....

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Levetiracetam Tablets USP 750 mg 120-count bottles Recalled by Aurobindo...

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Acetaminophen and Codeine Phosphate Tablets Recalled by Aurobindo Pharma USA...

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Acetaminophen and Codeine Phosphate Tablets Recalled by Aurobindo Pharma USA...

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Gabapentin Capsules Recalled by Aurobindo Pharma USA Inc. Due to CGMP...

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: DR. THAMES - LAP CHOLE Recalled by Applied Medical Resources Corp Due to...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Radiometer Medical ApS

Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...

The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Epix latis GRASPER Recalled by Applied Medical Resources Corp Due to There...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5 Part Number: 72202901...

The Issue: Space between the device and the packaging permits excessive movement which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Clip Applier Kit Recalled by Applied Medical Resources Corp Due to There may...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Bard Peripheral Vascular Inc

Recalled Item: Jamshidi Bone Marrow Biopsy/Aspiration Needle Recalled by Bard Peripheral...

The Issue: Sterility compromised due to packaging pouches that may not be sealed properly

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Rayner Intraocular Lenses Limited

Recalled Item: RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Recalled by Rayner...

The Issue: RaySert PLUS RSP01 LOT K030 labeled with an expiry of 2024-01 contained an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing