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 30, 2018

smith&nephew 5o (5 degree) GENESIS(R) II VALGUS BUSHING, REF CATALOG NUMBER 71440014 The GENESIS II Knee System…

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

Smith & Nephew, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 30, 2018

Synthes Torque Limiting Handle, Part Number 03.231.013 This device is used in systems indicated for fracture fixation.

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 23, 2018

Thoratec HeartMate 3 LVAS Implant Kit, Rx Only, Catalog # 106524US, 106524, 10652INT - LVAS KIT, HM 3 Indicated for…

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

Abbott

FDA (openFDA device enforcement)

Medical devices

Reported May 23, 2018

Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported May 23, 2018

DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manufactured and Distributed by eBars, LLC, Franklin, TN 37064…

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

eBars

12 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 23, 2018

Great Value Organic Ground Flax Seed, Net Wt. 16 oz. (1 LB) 454g. UPC 78742-14161, and Net Wt. 32 oz. (2 LB) 907g, UPC…

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

Healthy Food Ingredients

FDA (openFDA food enforcement)

Drugs

Reported May 23, 2018

Clindamycin 150 mg capsules, USP, 30-count M-Pak container. Mnfct by: Lannett Co. Inc., Philadelphia, PA. Mnfct for:…

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

Prescript Pharmaceuticals, Inc.

4 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported May 23, 2018

Tosoh ST AIA-PACK HbA1c, HbA1c Reagent, Pt. No. 025218 The device is designed for In Vitro Diagnostic Use Only for the…

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

Tosoh Bioscience Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 23, 2018

True Taste Seafood Hot Smoked Lake Herring; Ingredients: Lake Herring, salt, original smoke; To be weighed at point of…

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

True Taste, LLC.

6 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 23, 2018

Vans gluten free Original 6 WAFFLES NET WT 9 OZ (255g) INGREDIENTS:***VAN'S GLUTEN FREE MIX (BROWN RICE FLOUR, POTATO…

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

Tyson Foods Discovery Center

FDA (openFDA food enforcement)

Medical devices

Reported May 23, 2018

Philips Volcano CORE M2 Vascular System, Part # 400-0100.17, Rx Only. Used for the qualitative and quantitative…

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

Volcano Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 23, 2018

Persona Stemmed Tibial Provisional Size H Left, Item Number 42532108301 For use during orthopaedic surgery for…

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

Zimmer Biomet, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported May 18, 2018

Hempler Foods Group Recalls Ready-To-Eat Pepperoni Sticks Due to Misbranding and Undeclared Allergen

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

Hempler Foods Group LLC

USDA FSIS

Medical devices

Reported May 16, 2018

ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative…

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported May 16, 2018

BARD¿ BrachySource¿ Iodine125 radioactive seeds consist of a welded titanium capsule containing the I125 absorbed onto…

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

Bard Brachytherapy, Inc.

FDA (openFDA device enforcement)

Food

Reported May 16, 2018

Bob's Red Mill 100% Whole Wheat Bread Mix, Item 1674C194, packaged in flexible packaging bag, 4 bags to a cardboard…

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

Bob's Red Mill Natural Foods, Inc.

FDA (openFDA food enforcement)

Drugs

Reported May 16, 2018

Macroaggregated albumin (MAA) kit (for the preparation of Tc99m MAA), Aggregated and non-Aggregated Human Serum Albumin…

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

Coast Quality Pharmacy LLC

FDA (openFDA drug enforcement)

Medical devices

Reported May 16, 2018

Connecting Tube - Female to Male Luer Lock, HPCT8.8-60-M-FM Product Usage: The connecting tube is intended to be a…

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

Cook Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 16, 2018

BEQ-T 9410 Lurie Chldns Small 1/4, Custom Tubing Kit, Catalog No. 709000430

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

Datascope Corporation

27 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 16, 2018

MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in…

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

Diagnostic Hybrids, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 16, 2018

Fabius MRI, anesthesia machine, catalog no. 8607300 Product Usage: The products are inhalation anesthesia machines for…

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

Draeger Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 16, 2018

Eden's Ethnos Bulk Kratom 25 powder kilogram bag Also called K. Bali Supreme, K Maeng Da Supreme, K Green Vein, Green…

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

Eden's Ethnos, LLC

FDA (openFDA food enforcement)

Medical devices

Reported May 16, 2018

Hemodynamic monitoring system (HMS), comprised of a Patient Interface Module (Part Number 58401-000 and a User…

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 16, 2018

RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.

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

Mako Surgical Corporation

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.