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. 1,191 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,191 in last 12 months

Showing 2341–2360 of 51,434 recalls

FoodMay 28, 2025· Post Consumer Brands, LLC

Recalled Item: Post Honey Bunches of Oats with Almonds. Sweetened Cereal with Recalled by...

The Issue: Foreign Material (metal)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips eL18-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips eL18-4 EMT Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips L12-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips S7-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips C5-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Encore Medical, LP

Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...

The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips S5-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Encore Medical, LP

Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...

The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2025· Medtronic Navigation, Inc.-Boxborough

Recalled Item: O-arm O2 Imaging System. Mobile X-Ray System. Recalled by Medtronic...

The Issue: A mechanical component that supports the O2 gantry to the support structure...

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

Class II — Potential Health HazardOngoing
DrugMay 27, 2025· Torrent Pharma Inc.

Recalled Item: Fluoxetine Tablets Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 27, 2025· Torrent Pharma Inc.

Recalled Item: Fluoxetine Tablets Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 27, 2025· Fresenius Medical Care Holdings, Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Fresenius Medical Care Holdings,...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 27, 2025· Microbiologics Inc

Recalled Item: KWIK-STICK Recalled by Microbiologics Inc Due to Affected products were...

The Issue: Affected products were packaged with the incorrect KWIK STIK assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2025· GE Medical Systems, LLC

Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to GE HealthCare has...

The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2025· GE Medical Systems, LLC

Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to GE HealthCare...

The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2025· GE Medical Systems, LLC

Recalled Item: SIGNA PET/MR Recalled by GE Medical Systems, LLC Due to GE HealthCare has...

The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...

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

Class II — Potential Health HazardOngoing
DrugMay 23, 2025· Consumer Product Partners, LLC

Recalled Item: Spectrum Advanced Gel Hand Sanitizer Recalled by Consumer Product Partners,...

The Issue: Subpotent product: Product has cloudy appearance and tested below assay...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2025· Ascend Laboratories, LLC

Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories, LLC Due to...

The Issue: Failed Impurities/Degradation Specifications An out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2025· Ascend Laboratories, LLC

Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories, LLC Due to...

The Issue: Failed Impurities/Degradation Specifications An out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund