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. 2,659 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,659 in last 12 months

Showing 91819200 of 51,434 recalls

Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to 1. An...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to 1. An accessory may...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products NT-proBNP II Range Verifiers-For in vitro...

The Issue: May not meet the stability specifications for shelf life outlined in the...

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

Class III — Low RiskOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: BEQ-HMOD70000-USA/QUADROX-iD Recalled by Maquet Medical Systems USA Due to...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-iD Pediatric Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-iD Adult Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX -i Neonatal Recalled by Maquet Medical Systems USA Due to 1. An...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: BEQ-HMO 50000-USA/ QUADROX-i Small Recalled by Maquet Medical Systems USA...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Pediatric Recalled by Maquet Medical Systems USA Due to 1. An...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Small Adult Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX -i Neonatal Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
FoodMay 18, 2023· Werner Gourmet Meat Snacks, Inc.

Recalled Item: Chili Cacahuate Japones Recalled by Werner Gourmet Meat Snacks, Inc. Due to...

The Issue: Undeclared peanut

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2023· Aurolife Pharma, LLC

Recalled Item: Glycopyrrolate Tablets Recalled by Aurolife Pharma, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
FoodMay 17, 2023· HU PRODUCTS

Recalled Item: Hu Vanilla Crunch Dark Chocolate bar Recalled by HU PRODUCTS Due to...

The Issue: may contain undeclared tree-nuts

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 17, 2023· Beckman Coulter, Inc.

Recalled Item: Access Hybritech p2PSA reagent Recalled by Beckman Coulter, Inc. Due to...

The Issue: Reagent lot numbers include an insufficient concentration of blocking reagent.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Heartware, Inc.

Recalled Item: HeartWare Ventricular Assist Device System. a) Monitor 1521US Explore Tech...

The Issue: Medtronic has identified that the logfiles downloaded from the recently...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Draeger Medical Systems, Inc.

Recalled Item: Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale...

The Issue: The Resuscitaire Infant Radiant Warmer with the optional scale could display...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Aptio Automation Storage and Retrieval Module (SRM) Recalled by Siemens...

The Issue: A firmware error may lead to an incorrect association of test result(s) to a...

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

Class II — Potential Health HazardOngoing