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. 1,204 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,204 in last 12 months

Showing 8661–8680 of 30,923 recalls

Medical DeviceMarch 21, 2022· Breas Medical, Inc.

Recalled Item: Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS Recalled by...

The Issue: Ventilator mounting brackets for the Vivo 50/60/65 and Vivo 45LS ventilator...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2022· Avanos Medical, Inc.

Recalled Item: Avanos Cortrak 2 Enteral Access System (EAS) Recalled by Avanos Medical,...

The Issue: Product labeling is being modified. STOP using the Anonymous Account Mode...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2022· Acera Surgical Inc

Recalled Item: Restrata Recalled by Acera Surgical Inc Due to Misprinted expiration date on...

The Issue: Misprinted expiration date on the shelf-box

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2022· ROi CPS LLC

Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...

The Issue: A drug kit component was recalled by its manufacturer due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2022· Olympus Corporation of the Americas

Recalled Item: Ultrasonic Gastrovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: GF-UC140P-AL5 is no longer a compatible endoscope for reprocessing in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2022· ROi CPS LLC

Recalled Item: Convenience kits containing regard IV Start Kits: regard Clinical Packaging...

The Issue: A drug kit component was recalled by its manufacturer due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2022· ROi CPS LLC

Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...

The Issue: A drug kit component was recalled by its manufacturer due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2022· Hologic, Inc

Recalled Item: Panther Fusion GBS Assay Cartridges 96 Tests Recalled by Hologic, Inc Due to...

The Issue: Samples, run on a GBS Assay, that have analyte concentrations that are at or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2022· Intuitive Surgical, Inc.

Recalled Item: da Vinici X da Vinci Xi Sureform 45 Recalled by Intuitive Surgical, Inc. Due...

The Issue: As a result of complaint data review, it identified tissue pushout events...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2022· Carl Zeiss Meditec AG

Recalled Item: ZEISS miLOOP Lens Fragmentation Device . Used during cataract Recalled by...

The Issue: High friction of the slider can cause the device to stick, or not move as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2022· LetsGetChecked Inc.

Recalled Item: LetsGetChecked Blood Sample Collection kit-In vitro diagnostic medical...

The Issue: Users received sample collection kits that were assigned to another user....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2022· Stanbio Laboratory, LP

Recalled Item: Separation Technology Creamatocrit Plus Recalled by Stanbio Laboratory, LP...

The Issue: The device was being marketed as an IVD without a 510(k). Therefore,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Baxter Healthcare Corporation

Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...

The Issue: This correction is due to software anomalies occurring during use. If the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Baxter Healthcare Corporation

Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...

The Issue: This correction is due to software anomalies occurring during use. If the...

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

Class II — Potential Health HazardOngoing