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. 2,634 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,634 in last 12 months

Showing 62016220 of 49,990 recalls

Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) ENDO KIT Recalled by...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) BASIC NEURO Recalled...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) ANESTHESIA CIRCUIT...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) GYN CDS Recalled by...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) ENDO KIT Recalled by...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) C-SECTION CDS Recalled...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) MAJOR BREAST Recalled...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) ARTHROSCOPY Recalled...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· EBI, LLC

Recalled Item: 48" Lead Wires Recalled by EBI, LLC Due to Damage to the lead wire sheath...

The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· EBI, LLC

Recalled Item: Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for...

The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· Parker Laboratories, Inc.

Recalled Item: Redux Electrolyte Creme Recalled by Parker Laboratories, Inc. Due to Product...

The Issue: Product demonstrates low viscosity.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· Philips North America Llc

Recalled Item: Philips Patient Information Center (PIC) iX Uninterruptable Power Supply...

The Issue: Possible failure of Uninterruptable Power Supply (UPS) devices supporting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· EBI, LLC

Recalled Item: 20" Lead Wires Recalled by EBI, LLC Due to Damage to the lead wire sheath...

The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· EBI, LLC

Recalled Item: Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the...

The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...

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

Class II — Potential Health HazardOngoing
FoodMarch 21, 2024· AMY'S KITCHEN INC.

Recalled Item: Amy's Kitchen Enchilada Verde Whole Meal 10 oz. 12 pk Item # 000085 Recalled...

The Issue: L. mono contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2024· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Vancomycin Hydrochloride for Oral Solution Recalled by Amneal...

The Issue: Superpotent Drug: Due to overfilling of drug powder

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 21, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Rifampin Capsules USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2024· Apothecus Pharmaceutical Corp.

Recalled Item: VCF Vaginal Contraceptive Film (nonoxynol-9 Recalled by Apothecus...

The Issue: cGMP Diviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models:...

The Issue: Coolant level in the cooling circuit drops below a certain level, this may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Ontact Inc

Recalled Item: 24K Premium Lense Recalled by Ontact Inc Due to Contact lenses recalled due...

The Issue: Contact lenses recalled due to potential bacterial contamination.

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

Class II — Potential Health HazardOngoing