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. 1,165 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,165 in last 12 months

Showing 3081–3100 of 28,964 recalls

Medical DeviceSeptember 4, 2024· Olympus Corporation of the Americas

Recalled Item: Olympus Electrosurgical Generator Recalled by Olympus Corporation of the...

The Issue: There was an increase in complaints indicating an occurrence of system error...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline PEDIATRIC DRAPE PK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand medical procedure convenience kits Recalled by MEDLINE...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline DENTAL PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM1900 Recalled by LEICA BIOSYSTEMS...

The Issue: As part of our post market surveillance, we recognized that some customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand medical procedure convenience kits Recalled by MEDLINE...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Ambition S - For use as a diagnostic device Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: MR 7700 -For use as a diagnostic device to obtain cross-sectional images...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: MR 5300 - For use as a diagnostic device to obtain cross-sectional images...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Elition S -For use as a diagnostic device to Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: SmartPath to Ingenia Elition X - For use as a Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Ambition X - For use as a diagnostic device Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: SmartPath to dStream for 1.5T - For use as a Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Elition X- For use as a diagnostic device to Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Evolution Upgrade 3.0T - For use as a diagnostic device Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia 3.0T CX - For use as a diagnostic device Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: SmartPath to dStream for XR and 3.0T- For use as Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Centurion Sterile CirClamp Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Product has been identified as having holes in the packaging.

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

Class II — Potential Health HazardOngoing