All recall categories

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.

Medical devices

Reported Mar 6, 2019

Draco Enzymatic Deep-Cleaning Pads, Product Number HY0305Z Product Usage: Multi-tiered enzymatic detergent contains…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Madison Polymeric Engineering

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2019

Nita Crisp Spelt Bread Cracker, 8- & 16-ounce bags, In paper bags with a plastic window and has a re-closable ability…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nita Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 6, 2019

Ottogi Ramen Sari (Extra Noodle) 3.88oz x 48ea Item #21101009 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Ottogi America Inc.

16 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 6, 2019

Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Biomet Spine Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2019

AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 27, 2019

Snak Club Praline Pecans Made With Cane Sugar NET Wt. 2.25 oz (64 g) Produced By: Century Snack Commerce, CA 90040…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Century Snacks LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 27, 2019

Check-Flo Performer Introducer, Catalog Number RCFW-5.0-25-45-RB-CHB, GPN G11571

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cook Inc.

FDA (openFDA device enforcement)

Drugs

Reported Feb 27, 2019

tubby todd Bath Co, 100% NATURAL DREAM CREAM, Shea Butter and Mint, 3.5 FL OZ 99G, Distributed by: Tubby Todd Bath Co.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mariposa Labs LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 20, 2019

COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

AtriCure, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Feb 20, 2019

Labetalol 20mg, HCL, USP Injectable Solution, 20mg/4mL (5 mg per mL), 4mL single use syringe. Repackaged by Avella…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Avella of Deer Valley, Inc. Store 38

3 more products in this recall

FDA (openFDA drug enforcement)

Food

Reported Feb 20, 2019

Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Chicago Bar Company LLC Rxbar

18 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2019

Hemotherm CE Dual Reservoir Cooler/Heater, Model No. 400CE Product Usage: The HEMOTHERM¿ Model 400CE Dual Reservoir…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cincinnati Sub-Zero Products LLC, a Gentherm Company

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2019

Culinary Secrets, Butterscotch Instant Pudding Mix, Net Wt. 28 OZ, Marketed by Independent Marketing Alliance, Houston,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Diamond Crystal Brands, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2019

MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2019

OMNI K1 Broach Handle, Product Code HS-10054

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

OMNIlife science Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2019

Organic Sunflower Butter, Net Wt. 16 oz. (453g) Packaged under the following brand names: 1. Thrive Market, UPC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Oskri Corp.

19 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 20, 2019

Parent's Choice Toddler Next Stage¿ Milk Drink Powder Natural Milk Flavor With Other Natural Flavors, Stage 3, 1 Year…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

PBM Nutritionals, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2019

Ingenuity TF PET/CT (non-RoHS), Model Number 882456 This device is a diagnostic imaging system that combines Positron…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2019

Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems GmbH, DMC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2019

HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Magstim Company Limited

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2019

ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Ireland Diagnostics Division

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 13, 2019

Barcelona Nut Company, Roasted and Salted Select Inshell Pistachios 21/25, flexible package, shelf life of one year.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Barcelona Nut Company

FDA (openFDA food enforcement)

Medical devices

Reported Feb 13, 2019

BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature Sensing Infection Control Foley Catheter with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Medical Division

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.