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. 3,068 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,068 in last 12 months

Showing 12611280 of 30,923 recalls

Medical DeviceJuly 30, 2025· Contract Medical International GmbH

Recalled Item: Brand Name: Fortress Introducer Sheath System Product Name: Fortress...

The Issue: Units may have been packaged with an incorrect pouch label, which lists the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2025· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Clearview Strep A Exact II Dipstick Respiratory Kit Recalled by Mckesson...

The Issue: Due to a classification error in the inventory management system, specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales...

The Issue: VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Chemistry Products LAC Slides. Catalog Number: 8433880. 1 Sales Unit...

The Issue: VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2025· ORTOMA AB

Recalled Item: Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight Recalled by...

The Issue: Due to a weld breakage between the pin and inserter holder of the Inserter...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· Home Health US, Incorporated

Recalled Item: One Step Sterile Lancet for Single Use (3 sizes): 06949517008861 Recalled by...

The Issue: Due to incorrect/lack of Unique Device Identifier (UDI) codes.

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

Class III — Low RiskOngoing
Medical DeviceJuly 25, 2025· Zap Surgical Systems

Recalled Item: ZAP-X Radiosurgery System Recalled by Zap Surgical Systems Due to If the...

The Issue: If the radiosurgery system triggers a proximity error message during a long...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 25, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical convenience kits labeled as: 1. NEWBORN RESUSCITATION KIT...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 25, 2025· Merit Medical Systems, Inc.

Recalled Item: 10Fore Hemostasis Valve Catalog Number / UDI-DI code: MAPTEN4 / Recalled by...

The Issue: Due to a manufacturing issue involving the silicone quad ring where the ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· Olympus Corporation of the Americas

Recalled Item: Electrosurgical Recalled by Olympus Corporation of the Americas Due to...

The Issue: Potential for the ESG-410 Electrosurgical Generator to display an error...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· Olympus Corporation of the Americas

Recalled Item: Electrosurgical Recalled by Olympus Corporation of the Americas Due to...

The Issue: Potential for the ESG-410 Electrosurgical Generator to display an error...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· THOR Photomedicine Ltd

Recalled Item: Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Recalled by THOR...

The Issue: The potential for a failed welded nut to shear off. When this occurs, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2025· Dentsply IH, Inc.

Recalled Item: Brand Name: Atlantis IO FLO Product Name: Atlantis IO FLO-S Recalled by...

The Issue: The defect in the thread area will not allow the device to fully engage with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2025· Dentsply IH, Inc.

Recalled Item: Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Recalled by...

The Issue: The defect in the thread area will not allow the device to fully engage with...

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

Class II — Potential Health HazardOngoing