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. 2,851 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,851 in last 12 months

Showing 2452124540 of 30,923 recalls

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 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· 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 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 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: 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
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 11, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Nuclear gamma cameras (ADAC VERTEX PLUS/SOLUS/CARDIO Recalled by Philips...

The Issue: The firm was notified by a customer that the collimator exchange carriage...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2015· Toshiba American Medical Systems Inc

Recalled Item: INFX-8000V Interventional Angiography System. CAT-880B catheterization...

The Issue: The table base rotational brake that holds the table top may not always be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2015· Hummingbird Med

Recalled Item: ABG-HM-1 Hummi Micro Draw Blood Transfer Device Recalled by Hummingbird Med...

The Issue: Hummingbird Med Devices, Inc. is recalling the Hummi Micro Draw because of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece Recalled by Microtek...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH BELT Recalled by Microtek Medical Inc Due...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: LAPAROSCOPIC TUBING SET Recalled by Microtek Medical Inc Due to This recall...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY Recalled by...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing