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. 1,073 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,073 in last 12 months

Showing 12981–13000 of 49,990 recalls

Medical DeviceMarch 23, 2022· Medtronic Vascular, Inc.

Recalled Item: Medtronic IN.PACT AV Recalled by Medtronic Vascular, Inc. Due to Packaging...

The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2022· Medtronic Vascular, Inc.

Recalled Item: Medtronic IN.PACT Admiral Recalled by Medtronic Vascular, Inc. Due to...

The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: ACS Lap Chole Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: ACS IR - Angio Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: ACS Cath Lab Pack Recalled by American Contract Systems, Inc. Due to Product...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: 1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack Recalled by American...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· Steris Corporation

Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 2 Recalled by Steris...

The Issue: Product not approved for release for US distribution

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· Steris Corporation

Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5 Recalled by Steris...

The Issue: Product not approved for release for US distribution

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· Microbiologics Inc

Recalled Item: Inactivated macrolide-resistant Mycoplasma genitalium Recalled by...

The Issue: The QC process was not adequate for the specification range.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: 1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray Recalled by American...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2022· Varian Medical Systems Imaging Laboratory GmbH

Recalled Item: ARIA Radiation Therapy Management (RTM) VERSIONS 13.6 Recalled by Varian...

The Issue: Software issue for treatment plan and image management application may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2022· Breas Medical, Inc.

Recalled Item: Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS Recalled by...

The Issue: Ventilator mounting brackets for the Vivo 50/60/65 and Vivo 45LS ventilator...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2022· Avanos Medical, Inc.

Recalled Item: Avanos Cortrak 2 Enteral Access System (EAS) Recalled by Avanos Medical,...

The Issue: Product labeling is being modified. STOP using the Anonymous Account Mode...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2022· Acera Surgical Inc

Recalled Item: Restrata Recalled by Acera Surgical Inc Due to Misprinted expiration date on...

The Issue: Misprinted expiration date on the shelf-box

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

Class II — Potential Health HazardOngoing
DrugMarch 21, 2022· Adamis Pharmaceuticals Corporation

Recalled Item: SYMJEPI (epinephrine injection Recalled by Adamis Pharmaceuticals...

The Issue: Defective Delivery System: Potential clogging of the needle preventing the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: quinapril and hydrochlorothiazide tablets Recalled by Pfizer Inc. Due to...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: quinapril HCl/hydrochlorothiazide tablets Recalled by Pfizer Inc. Due to...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) tablets Recalled by Pfizer...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets Recalled by Pfizer...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets Recalled by Pfizer...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund