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 53615380 of 28,127 recalls

Medical DeviceOctober 12, 2023· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE Model Numbers BF-1TH190 Recalled by Olympus...

The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2023· Mc3 Inc

Recalled Item: NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal...

The Issue: May have increased water path restriction within the heat exchanger, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Randox Laboratories Ltd.

Recalled Item: RANDOX Total Bilirubin. Recalled by Randox Laboratories Ltd. Due to Randox...

The Issue: Randox has had reports of elevated patient results using Plasma (lithium...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Becton Dickinson & Company

Recalled Item: BD gravity sets (Product Name Recalled by Becton Dickinson & Company Due to...

The Issue: Affected infusion sets labeled as free of DEHP actually do contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Mc3 Inc

Recalled Item: NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal...

The Issue: May have increased water path restriction within the heat exchanger, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Unomedical A/S

Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...

The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Unomedical A/S

Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...

The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Medline manual resuscitators with integrated manometer Recalled by SunMed...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Becton Dickinson & Company

Recalled Item: BD Extension Sets (Product Name Recalled by Becton Dickinson & Company Due...

The Issue: Affected infusion sets labeled as free of DEHP actually do contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Becton Dickinson & Company

Recalled Item: BD Alaris Pump infusion sets (Product Name Recalled by Becton Dickinson &...

The Issue: Affected infusion sets labeled as free of DEHP actually do contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Curaplex manual resuscitators with integrated manometer Recalled by SunMed...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Unomedical A/S

Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...

The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 3400 Chemistry System Product Code 6844458 Running Software...

The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...

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

Class II — Potential Health HazardOngoing