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. 2,590 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,590 in last 12 months

Showing 1200112020 of 49,990 recalls

DrugJune 16, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Mometasone Furoate Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Defective Container

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various ob/gyn packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Angiography packs/trays Recalled by American Contract Systems, Inc....

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Breast Abdominoplasty Pack Recalled by American Contract Systems, Inc. Due...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various C-section packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various convenience packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various convenience packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: D&C pack Recalled by American Contract Systems, Inc. Due to Product was...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Port Insertion Packs Recalled by American Contract Systems, Inc. Due...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various eye packs Recalled by American Contract Systems, Inc. Due to Product...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various neurology packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Pacemaker Packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various ENT Packs Recalled by American Contract Systems, Inc. Due to Product...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Angiography/Cath Lab packs/trays Recalled by American Contract...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Cysto Packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various hysterectomy Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Laparoscopy Packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various PICC Line Recalled by American Contract Systems, Inc. Due to Product...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...

The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· NordicNeuroLab AS

Recalled Item: nordicBrainEX Recalled by NordicNeuroLab AS Due to When exporting merged...

The Issue: When exporting merged results from the BOLD, DSC, and DCE modules of...

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

Class II — Potential Health HazardOngoing