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. 2,728 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,728 in last 12 months

Showing 281300 of 28,964 recalls

Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) WCH...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens Recalled by Vortex...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) ROBOTIC Recalled...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: 25GA Subretinal Injection Cannula VS0220.25 Recalled by Vortex Surgical Inc....

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Tecfen Retractable Membrane Polisher Recalled by Vortex Surgical Inc. Due to...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical 25GA Backflush Recalled by Vortex Surgical Inc. Due to There...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical TID Pharos Illuminated Depressor Recalled by Vortex Surgical...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical I2 Injection Kit Recalled by Vortex Surgical Inc. Due to...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 Recalled by...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· Intuitive Surgical, Inc.

Recalled Item: da Vinci SP Recalled by Intuitive Surgical, Inc. Due to Access Port System...

The Issue: Access Port System tray may develop cracks potentially resulting in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· Hologic, Inc

Recalled Item: Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument....

The Issue: Presence of particulates in affected devices that can be deposited into...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10F Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Plum Duo Precision IV Pump Recalled by ICU Medical, Inc. Due to...

The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· LEASEIR TECHNOLOGIES SLU

Recalled Item: Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number:...

The Issue: The console label for affected devices is missing the "DANGER" symbol.

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

Class II — Potential Health HazardOngoing