Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 3,052 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,052 in last 12 months

Showing 40014020 of 30,923 recalls

Medical DeviceMay 22, 2024· Abbott Medical

Recalled Item: Abbott Infinity 5 Recalled by Abbott Medical Due to Their is a potential...

The Issue: Their is a potential that the implantable pulse generator replacement...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Abbott Medical

Recalled Item: Abbott Infinity 5 Recalled by Abbott Medical Due to Their is a potential...

The Issue: Their is a potential that the implantable pulse generator replacement...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Abbott Medical

Recalled Item: Abbott Infinity 7 Recalled by Abbott Medical Due to Their is a potential...

The Issue: Their is a potential that the implantable pulse generator replacement...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Thoratec Switzerland GMBH

Recalled Item: 2nd Generation CentriMag Primary Console Recalled by Thoratec Switzerland...

The Issue: Due to a component change, the console part of a circulatory support system...

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
Medical DeviceMay 21, 2024· Angiodynamics, Inc.

Recalled Item: IsoLoc Prostate Immobilization Treatment Balloon Device Kit Recalled by...

The Issue: A single batch of ISO-100 IsoLoc Gas-Release Endorectal Balloons is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products FS Diluent Pack 3 Recalled by Ortho-Clinical...

The Issue: VITROS Chemistry Products FS Diluent Pack 3, Lot 01-1645 may cause results...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2024· CareFusion 303, Inc.

Recalled Item: BD Alaris System Manager Recalled by CareFusion 303, Inc. Due to Due to a...

The Issue: Due to a software issue the PC unit may not connect to the server which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2024· Silkprousa LLC

Recalled Item: Pink Luminous Breast Recalled by Silkprousa LLC Due to Firm is marketing and...

The Issue: Firm is marketing and distributing the Pink Luminous Breast device without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for...

The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System Recalled by...

The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Siemens Healthcare Diagnostics Inc

Recalled Item: Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Recalled by...

The Issue: Siemens Healthineers has identified an issue with the RAPIDPoint500e system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...

The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...

The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Biomet, Inc.

Recalled Item: RingLoc Bi-Polar Hip System Acetabular Cup Recalled by Biomet, Inc. Due to...

The Issue: 41 mm acetabular outer heads were potentially assembled with a 42 mm locking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Cadwell Industries Inc

Recalled Item: Cascade IOMAX Cortical Module Recalled by Cadwell Industries Inc Due to...

The Issue: Electroneurodiagnostic medical device may contain a defective printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing