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.

7,509 stored notices name California, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach California too — those are in the archive.

Medical devices

Reported Mar 18, 2020

GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

SoundWave Professional Suite Software 3.2, Ref CI-6055-014, SPN 058-023-32085, UDI: (01)07630016853227, Logical…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Advanced Bionics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Bard Biopsy EnCor Probe, Stereotactic/Ultrasound 7G, REF number ECP017G, packaged individually in sterile pouches, 5…

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

Bard Peripheral Vascular Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Enzymatic Creatinine Reagent (CR-E 2 X 200), REF A60298, For in Vitro Diagnostic Use, Rx Only, UDI: 15099590625733

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

Beckman Coulter Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 11, 2020

Blendtopia Superfood Smoothie Kit Glow flavor, 7 oz flexible pouch

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

Blendtopia Products, LLC

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 11, 2020

CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)

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

CareFusion 303, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 11, 2020

Aminature L-Cysteine HCl Anhydrous 100 mesh 25KG DRUM

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

Cj Haide (Ningbo) Biotech Co., Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 11, 2020

Monitor for the Functional Imaging System for Magnetic Resonance Imaging System

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Remisol Advance running on hardware with Windows XP, Windows 7, Windows Server 2003 and Windows Server 2008 operating…

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

Normand-Info S.A.S.U.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

RespVent Closed Suction System T-Piece Tracheostomy Adult, Diameter: 4.6mm (14F), Length: 30.5cm (12in.), MDI Adapter,…

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

Respiratory Therapeutics Group LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Elecsys CA 19-9, Cat. No. 07027028190 - Product Usage: the product is an immunoassay for monitoring and management of…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009

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

Seca

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

bellavista 1000 ventilator, Catalog number 301.100.030. bellavista is an electronically controlled pneumatic…

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

Vyaire Medical

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2020

Protective Cover Vivo 55/65 (Used for Vivo 50/65), Part No. 006344. It is an accessory (i.e. protective cover) for the…

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

Breas Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2020

Annie Chun's Japanese Style Teriyaki Noodle Bowl with Cooked Hokkien Noodles - Sweet & Tangy sauce with Bok choy and…

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

CJ Foods Inc., A Division

FDA (openFDA food enforcement)

Medical devices

Reported Mar 4, 2020

Selenia Dimensions Mammography System, Model number ASY-04160, Selenia Dimensions Gantry, UDI 15420045505636,

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

Hologic, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2020

Lotte Choco Pie Cocao, 12 pack, 11.85 oz. (336 g) UPC: 8 801062 475148 Distributed by Lotte International America, Los…

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

Lotte Int'l America Corp.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 4, 2020

Getinge 46-Series Washer Disinfector Model # 46-4, Part Number:46-4-502 Product Usage: Used in facilities such as…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Maquet Cardiovascular US Sales, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2020

Medline HOI LUMBAR REF DYNJ902823G Lot 20AKA895 Expiration 2021-05-31 1 each GTIN (01)10193489219180

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

Medline Industries Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2020

Foodservice item, Norpac Catalog Number 08099, frozen FLAV-R-PAC Roasted Spicy Potatoes O'brien, 6/40 oz. (2.5 lbs.)…

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

PNW Veg Co. LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 4, 2020

ADVIA Chemistry Lipase, Ref. No. 01984894 B01-4840-01, Siemens Material No. 10311896, UDI 00630414482446 - Product…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2020

COHERENCE Oncologist, Model Nos. 07333680 & 07351898

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2020

Sierra Soups Pasta e Fagioli: All Natural Vegetarian Vegan (without pasta); Gluten Free (without pasta); Net Wt. 369 g…

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

Sierra Soups

FDA (openFDA food enforcement)

Medical devices

Reported Mar 4, 2020

Ellipse, Tiered-therapy Cardioverter/Defibrillator, REF (UDI/GTIN): CD1377-36QC (05414734507646), CD2411-36C…

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

St Jude Medical, Cardiac Rhythm Management Division

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.