Recalls distributed in California
These notices name California in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
7,403 stored notices name California, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,124 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported Aug 23, 2017
VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Brivo MR355, Optima MR360 Product Usage: The Brivo MR355/Optima MR360 is a whole body magnetic resonance scanner…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Plum 360 Infusion System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Kettle Brand Krinkle Cut Potato Chips Spicy Queso, 8.5 oz., Distributed by: Kettle Foods, Inc., Salem, OR 97301, UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kettle Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 23, 2017
Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,
High riskUsing this product could cause serious injury, illness or death — stop using it now.NatureAll-STF Holding, LLC
7 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 16, 2017
BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 16, 2017
Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.International Medsurg Connection, Inc.
58 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 16, 2017
Sorin Group Aortic Arch Cannula, 7 mm x 10 in x 3/8 in, Rx Only, Sterile Product Usage: The Aortic Arch Cannulae are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
FDA (openFDA device enforcement)
Reported Aug 16, 2017
PALLAS M/MAXIMIS 5.5 mm Instrument Tap. Part of MAXIMIS Pedicle Screw Spinal Fixation System. Valorem Surgical,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Valorem Surgical LLC
143 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2017
Luvo Inc. (USA) Recalls Poultry Products Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Luvo Inc. (USA)
USDA FSIS
Reported Aug 9, 2017
Corn Maiden Foods, Inc. Recalls Ready-to-Eat Beef Products Due To Misbranding
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Corn Maiden Foods, Inc.
USDA FSIS
Reported Aug 9, 2017
Testosterone Cypionate + Progesterone, 200 mg/ 2.5 mg/mL ,10 mL amber glass vials, Rx Only, Compounded by AXIA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Tomcat Instrument, REF ASY-07379, Hologic Incorporated, automated laboratory sample processing instrument.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Myelotec, Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Steamers in 5 Clams in Butter & Garlic Sauce, Goose Point brand. Product is packaged in a plastic tray with heat sealed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nisbet Oyster Co. Inc.
FDA (openFDA food enforcement)
Reported Aug 9, 2017
Black Beans Bonanza Tamales with black beans. No Dairy:
High riskUsing this product could cause serious injury, illness or death — stop using it now.Primavera Nueva
FDA (openFDA food enforcement)
Reported Aug 9, 2017
Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Professional Complementary Health Formulas, LLC
FDA (openFDA food enforcement)
Reported Aug 9, 2017
InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Aug 9, 2017
SoftLab Software Laboratory information system to be used in a medical research or clinical laboratory by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Soft Computer Consultants, Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 60…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Threshold Enterprises Ltd.
FDA (openFDA food enforcement)
Reported Aug 9, 2017
Lactulose Solution, USP, 10 g/15 mL, dose cups delivers 15 mL packaged in 50-unit dose cups per case, Manufactured by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
ROSA Brain, 3.0.0 The device is intended for the spatial positioning and orientation of instrument holders or tool…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.