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. 2,447 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,447 in last 12 months

Showing 2694126960 of 49,990 recalls

DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Testosterone Cypionate USP (Micronized) for prescription compounding...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Calcipotriene BP (Monohydrate) for prescription compounding Recalled by...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Nifedipine USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· Apace KY LLC

Recalled Item: Acyclovir Tablets Recalled by Apace KY LLC Due to Presence of Foreign...

The Issue: Presence of Foreign Tablet/Capsule; cartons labeled to contain Acyclovir...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 8, 2018· Vitalab Co Inc

Recalled Item: Product packaged in the following ways A) Sonne's Recalled by Vitalab Co Inc...

The Issue: The firm's vitamin C dietary supplement contains lactose, a milk-derived...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Stanbio Laboratory, LP

Recalled Item: Stanbio AC power adapter for the HemoPoint H2 meter Recalled by Stanbio...

The Issue: The US prong (type A) adapter plate may crack, break, or detach and remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT(R) ClearVUE(R) isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Flex - Model no. 728317 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT - Model no. 728306 Computed Tomography X-Ray system Recalled...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 - Model no. 728231 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT - Model no. 728332 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

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

Class II — Potential Health HazardOngoing