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. 2,696 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,696 in last 12 months

Showing 54815500 of 28,964 recalls

Medical DeviceOctober 5, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: Mobilett Mira wireless (VA20) mobile x-ray system(s) Recalled by Siemens...

The Issue: Due to the incorrect mounting of the buzzer component, there is no acoustic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Visgeneer, Inc.

Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...

The Issue: Due to products distributed without premarket clearance or approvals.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Visgeneer, Inc.

Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...

The Issue: Due to products distributed without premarket clearance or approvals.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: DENTEMP ONE STEP .077OZ Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Becton Dickinson Infusion Therapy Systems Inc.

Recalled Item: BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Recalled by...

The Issue: Over-the-needle, intravascular catheters may have needles that do not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: Acumen IQ Sensor with VAMP System Recalled by Edwards Lifesciences, LLC Due...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: TruWave Pressure monitoring set Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: FloTrac Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: TruWave with Vamp System Pressure monitoring set Recalled by Edwards...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: FloTrac Sensor with Vamp System Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: Acumen IQ Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: MEDIC's CHOICE CONTACT LENS SOLUTION 12FLOZ Recalled by Family Dollar...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: FIRST RESPONSE 2 CT Recalled by Family Dollar Stores, Llc. Due to Products...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: ARC TEETH WHITENING PEN 0.06 FL OZ Recalled by Family Dollar Stores, Llc....

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: ORAL B MOUTH SORE RINSE 237ML Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT Recalled by Family Dollar Stores,...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· St. Jude Medical

Recalled Item: CardioMEMS Patient Electronic System (PES) Recalled by St. Jude Medical Due...

The Issue: Potential for damaged and frayed power connector plug with repeated bending...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: GOODSENSE DENTURE CLEANSER GRN TAB 40CT Recalled by Family Dollar Stores,...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: AT HOME MARIJUANA TEST STRIP Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: FIXODENT ORG CREAM 2.4OZ Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing