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. 2,926 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,926 in last 12 months

Showing 1750117520 of 30,923 recalls

Medical DeviceMarch 13, 2018· LivaNova USA

Recalled Item: Inspire 6 Integrated Phisio OXY w/ HVR Reservoir Recalled by LivaNova USA...

The Issue: Some integrated sterile INSPIRE family products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2018· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments...

The Issue: The firm received complaints of drill bits breaking during use with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2018· Keystone Dental Inc

Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...

The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· McKesson Israel Ltd.

Recalled Item: McKesson Cardiology Hemo Recalled by McKesson Israel Ltd. Due to Change...

The Issue: Change Healthcare has identified an issue where, under certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Ohio Medical Corporation

Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...

The Issue: Final quality control testing was not completed before the devices were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· CooperSurgical, Inc.

Recalled Item: Fischer Cone Biopsy Excisor Recalled by CooperSurgical, Inc. Due to Products...

The Issue: Products have been packaged with an incorrect product size.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults...

The Issue: After two and a half years, the battery fuel gauge may indicate a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· CooperSurgical, Inc.

Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...

The Issue: Products have been packaged with the wrong Trocar length type.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker GmbH

Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...

The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...

The Issue: The power load floor plates which hold the ambulance cot anchors in place...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C3 Ventilator Unit Intended to provide ventilator support to adults...

The Issue: After two and a half years, the battery fuel gauge may indicate a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Zimmer Biomet, Inc.

Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...

The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C3 Ventilator Unit Product Usage: The HAMILTON-C3 ventilator is...

The Issue: An out of specification component on the control board may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C1 Ventilator Unit Product Usage: The HAMILTON-C1 ventilator is...

The Issue: An out of specification component on the control board may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2018· The Binding Site Group, Ltd.

Recalled Item: Binding Site Optilite Beta-2-Microglobulin Urine Kit Recalled by The Binding...

The Issue: The product is not meeting the antigen excess protection claim of up to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences EZ Glide Aortic Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula Recalled by SPS...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing