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.

Meat & poultry

Reported May 4, 2018

Eddy Packing Co., Inc. Recalls Smoked Sausage Products Due to Possible Foreign Matter Contamination

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

Eddy Packing Co., Inc.

USDA FSIS

Medical devices

Reported May 2, 2018

Accelerate PhenoTest BC kit, Ref #10101018. The firm name on the label is Accelerate Diagnostics, Tucson, AZ. A…

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

Accelerate Diagnostics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009 Used to achieve epithelial graft in the oral cavity.

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

Ace Surgical Supply Co., Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clariti…

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

CooperVision Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 -…

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

Covidien LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3), Product Code EVT45. Accessory Tips for use only with EVICEL…

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

Ethicon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee system devices are sterile, single-use…

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

Howmedica Osteonics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Oncomine Dx Target Test, (Model No. A32451), Oncomine Dx Target RNA/DNA Panel (Model No. A32441). A qualitative In…

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

Life Technologies Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional…

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

Sofradim Production

FDA (openFDA device enforcement)

Food

Reported May 2, 2018

Decorated (iced holiday cookies sold from self service cookie displays - cookies in the shape of eggs, bunnies and…

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

Whole Foods Market

FDA (openFDA food enforcement)

Food

Reported Apr 25, 2018

Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…

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

Divinity Product Distribution LLC

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 25, 2018

Buenas Grated coconut - frozen; Kinayod na Niyog Noix de Coco Rape; UPC: 4806514650443 Keep Frozen Net Wt. 16 oz.,…

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

Global Commodities Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

Stage-1 Tissue Punch, Disposable, 4.5mm; catalog number: ISS141K. Intended for use in partially or fully edentulous…

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

Keystone Dental Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 25, 2018

Human Fetal Hemoglobin (HBF-1) FITC Conjugate

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

Life Technologies Corporation

FDA (openFDA device enforcement)

Food

Reported Apr 25, 2018

Cali Green Malay Kratom all packages, all quantities

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

Nutrizone LLC

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the…

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

Siemens Medical Solutions USA, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 25, 2018

SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10514 8

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

Smucker Natural Foods, Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in…

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

Teleflex Medical Europe Ltd.

FDA (openFDA device enforcement)

Food

Reported Apr 25, 2018

HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g

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

The J.M. Smucker Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 18, 2018

Amaranth Flour, Organic Whole Grain, Item Number: 6001C224, Net wt. 22 oz. UPC 0 39978 00911 1. The label is read in…

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

Bob's Red Mill Natural Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 18, 2018

First aid/emergency kits containing Honeywell eyewash: CSM kit number Kit/cabinet Description CSM Eyewash# Size:…

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

Certified Safety Mfg Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

VOLISTA StandOP Surgical Light; Model numbers VLT600 SF AIM STP, VLT600 DF AIM STP, Ref. codes ARD568811901,…

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

Getinge US Sales LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and…

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

Hamilton Medical AG

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.