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 48,123 notices were distributed nationwide, so they reach California too — those are in the archive.

Medical devices

Reported Jan 8, 2020

O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000

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

Medtronic Navigation, Inc.-Littleton

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2020

NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact, high magnification image…

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

Nidek, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2020

Blood Glucose Monitoring System, Model Number 07400870001 ACCU-CHEK GUIDE SAMPLE KIT MG/DL - Product Usage: The…

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

Roche Diabetes Care, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2020

HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when…

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

Thoratec Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2020

Juno DRF, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of routine radiographs and…

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

Villa Sistemi Medicali S.P.A.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHBC100 - Product Usage: The device can assist…

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

Axis-Shield Diagnostics, Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

STA UNICALIBRATOR (ref. 00675)

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

Diagnostica Stago, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2020

R.H. Macys & Co. Roasted Salted Cherries Berries and Nuts with Dark Chocolate, in 10oz metal tin, UPC - 788709600362

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

Ferris Coffee and Nut Company, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2020

VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868

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

Mazor Robotics Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

7% BSA (Bovine Serum Albumin), Product Code: 8262487 - Product Usage: is used to dilute samples when assay values…

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

Ortho Clinical Diagnostics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

PTS Panels CHOL+HDL+GLU Test Strips, Reference Number 5412, for use on CardioChek PA or CardioChek Plus analyzers

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

Polymer Technology Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…

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

Allergan PLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

Alliance Tech Medical, Inc. All Flow Pulmonary Function Filters, 100 filters individually packaged in a clear, sealed…

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

Alliance Tech Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

QuickTox 5 Panel Drug Screen DipCard

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

Ameditech Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive cream for use with external electrodes -…

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

Bio-Signal Group Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2019

Hodgson Mill Unbleached All-Purpose White Wheat Flour 5 Lb bags 001042 Best By 10-01-2020 005517 Best By 10-02-2020

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

Cell-nique Corp. dba Living Harvest at Hudson River Foods

FDA (openFDA food enforcement)

Food

Reported Dec 25, 2019

Tri-Color Coleslaw - Marketside brand; 16 oz. plastic bag, SKU 3117 Colorful Coleslaw/Salade de Chou - President's…

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

Dole Fresh Vegetables Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 25, 2019

Siracha HOT Chili Sauce Net Wt. 28 oz. (1 lb. 12 oz.) (793 g); Net Wt. 17 oz. (1 Lb. 1 oz.) in PET Plastic bottles UPC:…

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

Huy Fong Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2019

Ascension¿ Silicone PIP-Silicone PIP Sz 1, Model Number: SPIP5201WW - Product Usage: The Ascension Silicone PIP implant…

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

Integra Lifesciences Sales LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

Medtronic Affinity, 38um Arterial Filter, Catalog number REF 351

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

Medtronic Perfusion Systems

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

Low Volume Cartridge IFU (SKU CAR-125-B) used with the following devices: 1) NxStage One, Model NX1000-1; 2) NxStage…

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

NxStage Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

A1CNow+ Systems (professional use product), Software Version Revision D, REF Numbers US: 3021, 3024; EU: 3037, 3038,…

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

Polymer Technology Systems

4 more products 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.