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.

7,516 stored notices name California, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,853 notices were distributed nationwide, so they reach California too — those are in the archive.

Medical devices

Reported May 24, 2017

Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument

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

Orthosoft, Inc. dba Zimmer CAS

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 24, 2017

RALEY'S MUESLI CHOCOLATE CURLCRUNCH CEREAL; 12 oz. box - foil bag inside paper box. UPC: 46567-02266;Product…

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

Raley's

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 24, 2017

Wingman 35 Crossing Catheter, 65cm, Model Numbers: WGM35065US WGM35065CE WGM35090US WGM35090CE WGM35135US WGM35135CE

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

ReFlow Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin…

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

Teleflex Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

VORTRAN Automatic Resuscitator, VARPlus; Model PTE-5002; Qty: 10 each Anesthesiology: This device is to be used by…

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

Vortran Medical Technology 1, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 24, 2017

Decorated (sugared) holiday cookies sold in the shape of purple eggs, pink bunnies or yellow chicks. These cookies were…

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

Whole Foods Market

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 24, 2017

Ziehm Imaging solo FD Mobile Fluoroscopic C-arm

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

Ziehm Imaging Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

NexGen Offset Stem Extension, sizes 14mm and 17mm For use in total arthroplasty.

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported May 20, 2017

FSIS Issues Public Health Alert For Imported Veal Products Due To Possible Non-O157 Shiga toxin producing E. coli…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Fsis

USDA FSIS

Meat & poultry

Reported May 18, 2017Updated Oct 23, 2026

The Osso Good Co. Recalls Beef and Pork Products Produced Without Benefit of Inspection

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

Yosemite Protein Products, Inc.

USDA FSIS

Medical devices

Reported May 17, 2017

Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box.…

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

Almore International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching

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

Arthrex, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Mentor Smooth Round SPECTRUM Post- Operatively Adjustable Saline Breast Implant, Product Code: 350-1490, UDI/GTIN:…

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

Mentor Texas, LP.

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is…

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Food

Reported May 17, 2017

Frozen Wild Shrimp Burgers, Wild Grill Foods brand, net wt. 12 oz. Each package contains 4/ 3 oz. pieces. UPC 8 94067…

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

Unisea Inc.

FDA (openFDA food enforcement)

Food

Reported May 17, 2017

Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin, 60 softgels Rx Only, Manufactured for: Vertical…

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

Vertical Pharmaceuticals, Inc.

FDA (openFDA food enforcement)

Meat & poultry

Reported May 13, 2017

Green Chile Food Company Retira Del Mercado Productos De Burrito Con Carne Y Aves Por Posible Contaminacin Con Listeria

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

Recalling firm not stated

USDA FSIS

Medical devices

Reported May 10, 2017

MR GHIATAS Beaded Breast Localization Wire, Product Code: 477201, 479201 Product Usage: The GHIATAS Beaded Breast…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2017

BD FlowSmart Set MiniMed Pro-set Rx Only Distributed by Medtronic MiniMed Inc. 8006464633 8185765555 Legal Manufacturer…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Food

Reported May 10, 2017

Beyond Beef Feisty Crumble Vegan Gluten-free Non-GMO Weight: 10 lbs. (2) 5 lb. bags UPC: 10852629004412 KEEP FROZEN 111…

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

Beyond Meat

FDA (openFDA food enforcement)

Medical devices

Reported May 10, 2017

Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707…

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

Richard-Allan Scientific Company

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2017

Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…

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

Roche Diabetes Care, Inc.

FDA (openFDA device enforcement)

Food

Reported May 10, 2017

Whole Foods Market Cold Pressed Juice, Apple; 16 FL. Oz. (1 pt) 473 mL. Keep refrigerated - Enjoy within 5 days of…

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

Urban Remedy

FDA (openFDA food 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.