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. 1,100 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,100 in last 12 months

Showing 7781–7800 of 49,990 recalls

DrugOctober 2, 2023· Pine Pharmaceuticals, LLC

Recalled Item: Tropi-Phen (Tropicamide 1% phenylephrine HCl 2.5%) ophthalmic solution...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2023· Pfizer Inc.

Recalled Item: 2% Lidocaine HCl Injection Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: identified as glass.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 2, 2023· Coapt LLC

Recalled Item: Coapt ControlSeal Electrode Recalled by Coapt LLC Due to Patient may...

The Issue: Patient may experience minor burn or blistering if device is exposed to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Coapt LLC

Recalled Item: Coapt Dome Electrode Recalled by Coapt LLC Due to Patient may experience...

The Issue: Patient may experience minor burn or blistering if device is exposed to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III Gastrointestinal Videoscope Recalled by Olympus Corporation...

The Issue: Sterilization failures when devices are sterilized per the Reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Carestream Health, Inc.

Recalled Item: The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray Recalled...

The Issue: There is a potential for unexpected failure of the electrical components...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Carestream Health, Inc.

Recalled Item: DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due...

The Issue: Unexpected failure of electrical components within the CPI generator.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Stanbio Laboratory, LP

Recalled Item: STAT-Site M BHB Test Strips Recalled by Stanbio Laboratory, LP Due to...

The Issue: Deterioration in the stability of the Test Strips results in diminished...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Edge Biologicals Inc

Recalled Item: Edge Biologicals STERILE WATER Recalled by Edge Biologicals Inc Due to Due...

The Issue: Due to product outer packaging incorrectly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Sentinel CH SpA

Recalled Item: Alinity c Iron Reagent Recalled by Sentinel CH SpA Due to A high recovery of...

The Issue: A high recovery of Iron assay has been observed at some customer sites....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Atrium Medical Corporation

Recalled Item: Atrium Firm PVC Thoracic Catheter 36FR Straight Recalled by Atrium Medical...

The Issue: A sterilization nonconformance prematurely aged the product, resulting in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Sentinel CH SpA

Recalled Item: IRON assay Recalled by Sentinel CH SpA Due to A high recovery of Iron assay...

The Issue: A high recovery of Iron assay has been observed at some customer sites....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing