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 48,122 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported Jun 15, 2022
Tacrolimus (Brand Capsules ) 0.5 mg/mL Suspension, Rx, This is a compounded medication., Valor Compounding Pharmacy,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Valor Compounding Pharmacy, Inc. dba Valor Compounding Pharmacy
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jun 15, 2022
Van Leeuwen Ice Cream -Oat Milk Brown Sugar Chunk - 14 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Van Leeuwen Ice Cream
FDA (openFDA food enforcement)
Reported Jun 8, 2022
FIRMap" Catheter, 60mm Basket
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott
FDA (openFDA device enforcement)
Reported Jun 8, 2022
BBU Fine Whole Wheat Flour Bulk-AA-50251, Bulk Tanker; SG Whole Wheat Fine Flour 2,000 lb. Tote-AA Storage instructions…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ardent Mills, LLC
FDA (openFDA food enforcement)
Reported Jun 8, 2022
In-Line ventilator adaptor
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corporation
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2022
BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific reagent for the Anti-Kappa antibody, which specifically…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2022
DYNEX Agility, Agility Analyzer, Model No. 67000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dynex Technologies, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2022
The C304-HIS device features a guide wire to access the vein, a valve to reduce blood loss during the implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Jun 8, 2022
PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MicroPort Orthopedics Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2022
Cherry Coca-Cola Zero Sugar Case UPC: 0 49000 04751 6 12 pack fridge pack Single 12 oz. cans if sold individually from…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reyes Coca-Cola Bottling, LLC
FDA (openFDA food enforcement)
Reported Jun 8, 2022
JIF CREAMY PEANUT BUTTER packaged in 18gram, 500gram, 1 kilogram, 1.1oz (120 count)12oz, 16oz, 28oz, 40oz, 48oz, 4lb…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The JM Smucker Company LLC
23 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2022
Jason & Mary Large Milk Peanut Butter Cup
High riskUsing this product could cause serious injury, illness or death — stop using it now.Walnut Creek Chocolate Co. Inc.
14 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2022
XVIVO Organ Chamber REF 19020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xvivo Perfusion Ab
FDA (openFDA device enforcement)
Reported Jun 1, 2022
The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 receptor blockade. Substances known to specifically…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accriva Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Cole's Select Curry Salmon Rice Bowl, Green Curried Salmon Over Jasmine Rice, Net Wt. 8 oz., UPC 19962022057
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Colewillaidan LLC
FDA (openFDA food enforcement)
Reported Jun 1, 2022
SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market unit contains 10 individual wafers.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Higher Education Make Out Ready Vegan Lip Balm, SPF 15, Net Wt. 0.15 oz (4.25 g) per tube, Active Ingredients:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Eco Lips, Inc.
FDA (openFDA drug enforcement)
Reported Jun 1, 2022
Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System; The device is placed in a plastic tray with a snap on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Losartan Potassium & HCTZ Tablets 50mg/12.5 mg, hydrochlorothiazide USP 12.5, Pkg Size: 90, NDC: 68788-7758-09.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jun 1, 2022
INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Orthopaedics GmbH
FDA (openFDA device enforcement)
Reported Jun 1, 2022
(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
AC-powered adjustable medical beds with built-in electric DC actuators and controls.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Umano Medical, Inc.
1 more product in this recall
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.