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. 2,702 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,702 in last 12 months

Showing 46214640 of 51,434 recalls

FoodSeptember 3, 2024· Blue Tape Sriracha

Recalled Item: Blue Tape Sriracha sauce is condiment Recalled by Blue Tape Sriracha Due to...

The Issue: Acidified product was manufactured by firm without ODA license.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2024· Ascend Laboratories, LLC

Recalled Item: Mycophenolic Acid Delayed-Release Tablets USP Recalled by Ascend...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 1, 2024· SIN SISTEMA DE IMPLANTE NACIONAL S.A

Recalled Item: Implant Epikut S Plus CM 16-Degrees 4 Recalled by SIN SISTEMA DE IMPLANTE...

The Issue: Dental implant box incorrectly labels the diameter as 4,5 X 18,0 mm, but the...

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

Class II — Potential Health HazardOngoing
DrugAugust 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Mupirocin Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2024· Hammond's Candies Since 1920 II, LLC

Recalled Item: Hammond's Dark Chocolate Filled Mini Waffle Cones Recalled by Hammond's...

The Issue: Undeclared allergen: milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 30, 2024· Philips North America

Recalled Item: IntelliVue Patient Monitor MX400 (Model Number 866060) Recalled by Philips...

The Issue: During a production process, Philips became aware of one IntelliVue power...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Stryker Neurovascular

Recalled Item: The Trevo Trak 21 Microcatheter is a single-lumen Recalled by Stryker...

The Issue: Stryker Neurovascular has observed that devices with Out of United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Blue Ortho

Recalled Item: Predict+ is a data-driven Recalled by Blue Ortho Due to Predict+ is being...

The Issue: Predict+ is being recalled for lack of pre-market clearance/approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Melrose Wakefield Hospital Injector And Syringe Recalled by Merit Medical...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar MAP152 AssessPLUS Large Bore Hemostasis...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar MAP302 Honor Hemostasis Valve Metal...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar MAP403 MBA Hemostasis Valve Metal...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE Automatic Digital Blood Pressure Monitor Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device MAP 112 Access-9 Large Bore Hemostasis Value...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar Injector And Syringe Recalled by Merit...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to The...

The Issue: The software has anomalies that have the potential to cause alarms,...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2024· Wilson-Cook Medical Inc.

Recalled Item: Cook Medical Hemo-7 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook...

The Issue: Specific lots of product have been manufactured with nonconforming raw...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· Microcare Medical

Recalled Item: Good Vibrations Ultrasonic Cleaner Solution Recalled by Microcare Medical...

The Issue: Contaminated equipment and packaging caused Klebsiella oxytoca, Enterobacter...

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

Class II — Potential Health HazardOngoing