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. 1,020 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,020 in last 12 months

Showing 43561–43580 of 56,506 recalls

Medical DeviceMarch 13, 2015· Lusys Laboratories, Inc.

Recalled Item: Ebola GP IgM Blood (Blood Serum/Plasma/Cassette) Recalled by Lusys...

The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2015· Lusys Laboratories, Inc.

Recalled Item: Ebola VP-40 IgG/IgM (Blood Serum/Plasma/Cassette) Recalled by Lusys...

The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2015· Lusys Laboratories, Inc.

Recalled Item: Ebola Virus Antigen Nasal Recalled by Lusys Laboratories, Inc. Due to LuSys...

The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2015· Lusys Laboratories, Inc.

Recalled Item: Ebola IgX VP-40 Serum/Plasma/Blood Cassette Recalled by Lusys Laboratories,...

The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2015· Teleflex Medical

Recalled Item: Pluer-evac Sahara Chest Drainage System Recalled by Teleflex Medical Due to...

The Issue: Package contains incorrect sized unit: The adult sized S-1100-08LF product...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2015· Lusys Laboratories, Inc.

Recalled Item: Ebola Virus Antigen Blood Recalled by Lusys Laboratories, Inc. Due to LuSys...

The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2015· Vital Signs Colorado Inc.

Recalled Item: CareFusion Vital Signs LightWand Stylet. A device inserted into an Recalled...

The Issue: Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2015· Pointe Scientific, Inc.

Recalled Item: Pointe Scientific autoHDL Reagent H7545 H7545-R1 in a bulk cube Recalled by...

The Issue: Crystals may be observed in the R1 reagent. Crystals may be a result of the...

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

Class III — Low RiskOngoing
Medical DeviceMarch 13, 2015· Lusys Laboratories, Inc.

Recalled Item: Ebola Accessories assembled Recalled by Lusys Laboratories, Inc. Due to...

The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2015· Bard Peripheral Vascular Inc

Recalled Item: Denali Filter-Jugular/Subclavian DL950J Denali Filter-Femoral Delivery...

The Issue: IFU missing contraindications: Patients with uncontrolled sepsis and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2015· Lusys Laboratories, Inc.

Recalled Item: Ebola Virus GP-VP IgS Recalled by Lusys Laboratories, Inc. Due to LuSys...

The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2015· Vital Signs Colorado Inc.

Recalled Item: Introduction Pack. A device inserted into an endotracheal tube to Recalled...

The Issue: Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Nuclear Gamma Cameras (ADAC Vertex Classic Recalled by Philips Medical...

The Issue: During clinical use of a Vertex Plus Gamma Camera, as the detector heads...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2015· Lusys Laboratories, Inc.

Recalled Item: Ebola GP IgX Blood Recalled by Lusys Laboratories, Inc. Due to LuSys...

The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2015· Biomet Spine, LLC

Recalled Item: Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage:...

The Issue: Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· Biomet Spine, LLC

Recalled Item: Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 P_roduct...

The Issue: Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· CareFusion 303, Inc.

Recalled Item: Alaris PC units Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the Alaris PC unit because of an error code. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network Recalled by Mindray DS USA, Inc. dba...

The Issue: Software anomaly in the Panorama System software version 8.9 that manifests...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· Biomet Spine, LLC

Recalled Item: Polaris 4.75 TI Spinal System Recalled by Biomet Spine, LLC Due to...

The Issue: Multiaxial screws may not meet internal requirements related to fatigue...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to GE Healthcare has recently...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing