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. 2,489 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,489 in last 12 months

Showing 3402134040 of 51,434 recalls

Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Conserve Cups: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Conserve Shells: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Lineage Shell: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Lineage Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· Omega Medical Imaging, Inc.

Recalled Item: 2 over 2 Elevating Monitor Suspension - Omega Medical Imaging Recalled by...

The Issue: Elevating Monitor Suspension separated from the lifting column bracket

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2016· Encore Medical, Lp

Recalled Item: MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES Recalled by...

The Issue: Reported failure of the instrument. The retaining ring component of a neck...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2016· Invacare Corporation

Recalled Item: Invacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16 AW. Packed...

The Issue: The rear gradation scale was screen printed upside down on the flowmeter gauge.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2016· Invacare Corporation

Recalled Item: lnvacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16. Packed one...

The Issue: The rear gradation scale was screen printed upside down on the flowmeter gauge.

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

Class II — Potential Health HazardOngoing
FoodJune 20, 2016· Meduri Farms Inc

Recalled Item: Meduri Farms Dried Blueberries/Sugar Infused Recalled by Meduri Farms Inc...

The Issue: Meduri Farms Dried Blueberries/Sugar Infused product is recalled due to a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 20, 2016· Medtronic Navigation

Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...

The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2016· Karl Storz Endoscopy

Recalled Item: Image1 SPIES X-LINK Camera Control Unit (CCU) Recalled by Karl Storz...

The Issue: Potential electrical interference issue when the Image1 SPIES X-LINK and...

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

Class II — Potential Health HazardOngoing
DrugJune 17, 2016· Teva North America

Recalled Item: ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL)...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Linezolid Injection 600 mg/300 mL Rx Only Recalled by Teva North America Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Ondansetron Injection USP 40 mg/20 mL (2 mg/mL) Recalled by Teva North...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 17, 2016· Annona Company, LLC

Recalled Item: Earnest Eats Chewy Granola Dark Chocolate Almond .2 Recalled by Annona...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 17, 2016· Integra LifeSciences Corp.

Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...

The Issue: Data from internal studies suggests there may be a potential that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2016· Ab Sciex

Recalled Item: AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part...

The Issue: MultiQuant MD software where under certain conditions a user can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2016· Ab Sciex

Recalled Item: AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro...

The Issue: MultiQuant MD software where under certain conditions a user can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2016· Ab Sciex

Recalled Item: AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro...

The Issue: MultiQuant MD software where under certain conditions a user can be...

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

Class II — Potential Health HazardOngoing