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. 2,644 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,644 in last 12 months

Showing 37613780 of 28,127 recalls

Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Integra LifeSciences Corp.

Recalled Item: CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical...

The Issue: Potential for the CUSA Excel 23KHz Straight Handpiece housing to crack, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Baxter Healthcare Corporation

Recalled Item: Life2000 Ventilator Recalled by Baxter Healthcare Corporation Due to...

The Issue: Potential for certain Life2000 ventilator systems to either fail to charge...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2024· Artivion, Inc

Recalled Item: (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch Recalled...

The Issue: Grafts were found to have been approved, released, shipped and implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2024· Artivion, Inc

Recalled Item: CryoValve SG Pulmonary Human Heart Valve Recalled by Artivion, Inc Due to...

The Issue: Grafts were found to have been approved, released, shipped and implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-FR Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-V Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-CR Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to LIH Influence check...

The Issue: LIH Influence check settings for Lipemia are incorrect which may result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2024· CUE HEALTH INC

Recalled Item: Cue Health COVID-19 Test Cartridge Cue COVID-19 Test Recalled by CUE HEALTH...

The Issue: Due to modified test kits being marketed and distributed without FDA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2024· WOM World Of Medicine AG

Recalled Item: WOM Tube Set for lrrlgatlon Recalled by WOM World Of Medicine AG Due to...

The Issue: Incorrect transponder data was written on the RFID tags triggers the error...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2024· Alcon Research LLC

Recalled Item: Surgical Image Guidance Functionality Recalled by Alcon Research LLC Due to...

The Issue: After surgery initiation, while using surgical image guidance, if...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2024· Howmedica Osteonics Corp.

Recalled Item: Gray Revision Instrument System Accessory Tray/Case Recalled by Howmedica...

The Issue: The design of the HRIS Storage & Sterilization Case and Tray P/N 6210-9-900...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2024· Howmedica Osteonics Corp.

Recalled Item: HRIS Storage & Sterilization Case and Tray Recalled by Howmedica Osteonics...

The Issue: The design of the HRIS Storage & Sterilization Case and Tray P/N 6210-9-900...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: When a DxI 9000 Access Immunoassay Analyzer is connected to a Laboratory...

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

Class II — Potential Health HazardOngoing