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. 2,724 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,724 in last 12 months

Showing 681700 of 51,434 recalls

FoodNovember 18, 2025· Karabetian Import and Distribution, Inc.

Recalled Item: Product: Zimi Puff Pastry French Style (frozen) Package Size and Recalled by...

The Issue: partially hydrogenated oils (PHOs) in foods exported to the US

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Nebivolol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 18, 2025· AGFA Healthcare Corp.

Recalled Item: Brand name: AGFA Digital Radiography X- Ray system DR 800 Recalled by AGFA...

The Issue: It is possible to exceed the maximum allowed Air Kerma rate (AKR) of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2025· Instrumentation Laboratory

Recalled Item: HemosIL SynthAFax. Partial Thromboplastin Time Tests. Recalled by...

The Issue: Recalled lots were manufactured with double the amount of preservative...

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

Class III — Low RiskOngoing
Medical DeviceNovember 18, 2025· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Hardware configuration of the BeneVision Central Monitoring System (CMS)...

The Issue: When the Worstation of the BeneVision DMS has a specific hardware...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2025· DICOM Grid, Inc.

Recalled Item: Intelerad InteleShare software Recalled by DICOM Grid, Inc. Due to Software...

The Issue: Software intended to aid in diagnosing conditions, planning treatments,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number:...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers:...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· Sophysa

Recalled Item: The Pressio 2 ICP Monitoring System Recalled by Sophysa Due to Customer...

The Issue: Customer complaints of Pressio monitor rebooting.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· Sheathing Technologies Inc

Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...

The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Orthofix NorthStar OCT Navigation Surgical Technique Guide Recalled by...

The Issue: The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly...

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

Class II — Potential Health HazardOngoing
FoodNovember 16, 2025· Prime Food Processing LLC.

Recalled Item: Lava Bun with Salted Egg Yolk orange packaging (Frozen) Unsalted Recalled by...

The Issue: Products do not declare milk in the Contains statement or the ingredient...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 16, 2025· Prime Food Processing LLC.

Recalled Item: Lava Bun with Green Tea Flavor bright lime green packaging Recalled by Prime...

The Issue: Products do not declare milk in the Contains statement or the ingredient...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
DrugNovember 14, 2025· Cipla USA, Inc.

Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2025· Cipla USA, Inc.

Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund