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. 2,689 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,689 in last 12 months

Showing 67016720 of 51,434 recalls

Medical DeviceFebruary 15, 2024· Philips North America Llc

Recalled Item: DIVA 24 Inch Widescreen LCD Touch Display - Used with Recalled by Philips...

The Issue: If the DIVA touch display generates touch inputs without user interaction,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Mariner RDX Polyaxial Head Recalled by SEASPINE ORTHOPEDICS CORPORATION Due...

The Issue: Screw heads, of pedicle screw systems, have thin lead-in thread that pose a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Masimo Corporation

Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...

The Issue: Their is a potential that Oximeter may automatically power off and on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2024· Bio-Rad Laboratories

Recalled Item: Bio-Rad Recalled by Bio-Rad Laboratories Due to Due to incorrect...

The Issue: Due to incorrect calibrations and controls, their is a potential of...

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

Class II — Potential Health HazardOngoing
DrugFebruary 14, 2024· Golden State Medical Supply Inc.

Recalled Item: Fluticasone Propionate Nasal Spray USP Recalled by Golden State Medical...

The Issue: CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2024· Covidien, LP

Recalled Item: Signia" Small Diameter Curved Tip Intelligent Reload Recalled by Covidien,...

The Issue: Under certain firing conditions, reloads were found to articulate in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2024· Covidien, LP

Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload Recalled by...

The Issue: Under certain firing conditions, reloads were found to articulate in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2024· Randox Laboratories Ltd.

Recalled Item: Cystatin C Calibrator - In vitro diagnostic (IVD) use in Recalled by Randox...

The Issue: Cystatin C Calibrator Series CVS 2699, is running with a negative bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2024· Baxter Healthcare Corporation

Recalled Item: STERIS Boot Assembly Recalled by Baxter Healthcare Corporation Due to Three...

The Issue: Three lots of the Boot Assembly, Traction Device are being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2024· HeartSine Technologies Ltd

Recalled Item: HeartSine samaritan PAD (Public Access Defibrillator): Type/Catalog: SAM...

The Issue: Automated external defibrillators were shipped in their test configuration...

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

Class II — Potential Health HazardOngoing
FoodFebruary 13, 2024· AMY'S KITCHEN INC.

Recalled Item: Gluten Free Bean and Cheese Burrito (5.5 oz) Recalled by AMY'S KITCHEN INC....

The Issue: Presence of foreign material in food (plastic)

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2024· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Oseltamivir Phosphate for Oral Suspension 6mg/ml Recalled by Amneal...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification test results.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2024· FA Online Inc

Recalled Item: ForeverMen Natural Energy Boost Capsules Recalled by FA Online Inc Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 12, 2024· MCKESSON CORPORATION

Recalled Item: CABTREO (clindamycin phosphate Recalled by MCKESSON CORPORATION Due to CGMP...

The Issue: CGMP Deviations: Product was stored outside labeled storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2024· Micro Labs Limited

Recalled Item: Clobazam Tablets 10mg Recalled by Micro Labs Limited Due to CGMP Deviations:...

The Issue: CGMP Deviations: Out of specification for residual solvents.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 12, 2024· Sarnova HC, Llc

Recalled Item: Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a Recalled...

The Issue: Endotracheal Tube Holder included in certain kits is not compatible with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2024· ARROW INTERNATIONAL Inc.

Recalled Item: ARROW QuickFlash Radial Artery Catherization (wire Recalled by ARROW...

The Issue: Teleflex is initiating this voluntary recall for the above-mentioned...

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

Class I — Serious Health HazardOngoing