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 461480 of 30,923 recalls

Medical DeviceNovember 21, 2025· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Emphasizing instructions for LVP duration programming located in the IFU.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2025· Medline Industries, LP

Recalled Item: Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK Recalled...

The Issue: Firm received multiple complaints regarding tubing disconnecting from oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2025· Roche Diagnostics Operations, Inc.

Recalled Item: The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay...

The Issue: Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2025· Medtronic Neuromodulation

Recalled Item: Restore Clinician Programmer Application (CP App) Recalled by Medtronic...

The Issue: Software issue where a Device Reset message displayed on the app was unable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2025· Steris Corporation

Recalled Item: AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product...

The Issue: Wire connected to the electrical box may shift out of its intended position,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2025· Steris Corporation

Recalled Item: AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product...

The Issue: Wire connected to the electrical box may shift out of its intended position,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2025· AGFA Healthcare Corp.

Recalled Item: Brand name: AGFA Digital Radiography X- Ray system DR 800 Recalled by AGFA...

The Issue: It is possible to exceed the maximum allowed Air Kerma rate (AKR) of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2025· Instrumentation Laboratory

Recalled Item: HemosIL SynthAFax. Partial Thromboplastin Time Tests. Recalled by...

The Issue: Recalled lots were manufactured with double the amount of preservative...

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

Class III — Low RiskOngoing
Medical DeviceNovember 18, 2025· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Hardware configuration of the BeneVision Central Monitoring System (CMS)...

The Issue: When the Worstation of the BeneVision DMS has a specific hardware...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2025· DICOM Grid, Inc.

Recalled Item: Intelerad InteleShare software Recalled by DICOM Grid, Inc. Due to Software...

The Issue: Software intended to aid in diagnosing conditions, planning treatments,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number:...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers:...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· Sophysa

Recalled Item: The Pressio 2 ICP Monitoring System Recalled by Sophysa Due to Customer...

The Issue: Customer complaints of Pressio monitor rebooting.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· Sheathing Technologies Inc

Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...

The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Orthofix NorthStar OCT Navigation Surgical Technique Guide Recalled by...

The Issue: The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing