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. 2,662 recalls have been distributed to California in the last 12 months.
Showing 43561–43580 of 56,506 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Captopril Tablets Recalled by Wockhardt Usa Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: out of specification for thickness.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BADIA Ground Cumin Recalled by Badia Spices, Inc. Due to Undeclared Peanut
The Issue: Undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cinnamon Almonds Recalled by Trader Joes Company Due to Undeclared Peanuts
The Issue: Trader Joes Company is recalling its 16 ounce packages of Trader Joes...
Recommended Action: Do not consume. Return to store for a refund or discard.
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.
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.
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.