Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,660 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,660 in last 12 months

Showing 30213040 of 28,127 recalls

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 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 CV ANESTHESIA - ROOM SET UP Recalled by MEDLINE INDUSTRIES, LP -...

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: Centurion brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to It...

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· 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· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM1100 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· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM1850 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· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM3050 S 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· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM1510 S 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· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM1950 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· Howmedica Osteonics Corp.

Recalled Item: Triathlon Universal TS Baseplate Size 2 - A single use Recalled by Howmedica...

The Issue: Anterior locking tabs on the Triathlon Universal Baseplate are out of...

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
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· 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: 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: 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: 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 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: 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