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 48,828 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported Apr 21, 2021
Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device, UDI: (01) 00858701006049…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Apr 15, 2021
Olymel S.E.C./L.P. Recalls Ready-to-Eat Ham Products Due to Possible Salmonella Enteritidis Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olymel S.E.C./L.P.
USDA FSIS
Reported Apr 14, 2021
Anand Far Far (Garlic Sandige) Net Weight 7 oz./200 g package ingredients: rice, wheat flour, garlic, red chilli,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Babco Foods International, LLC
FDA (openFDA food enforcement)
Reported Apr 14, 2021
Amicus MNC Apheresis Kit - Double Needle - Product Usage: intended for use in the collection of blood components and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fenwal Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Synapse PACS - Radiological Image Processing System - Product Usage: intended for use, as a web based application, on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fujifilm Medical Systems U.S.A., Inc.
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Drop Arm Versamode"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gf Health Products
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Panther Fusion Tube Tray, REF PRD-04000, PN: FA-15004, Cont. 18 Tube Trays - Product Usage: an ancillary consumable to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Roasted Salted In shell Pistachios 3 lb. bag, 25 lb cartons, 30 lb. cartons, 50 lb. sacks, 2,000 lb. sacks, 2,200 lb…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Horizon Nut Company, LLC
FDA (openFDA food enforcement)
Reported Apr 14, 2021
Trial Cutting Guide for Triathlon Total Knee System, Triathlon PKR System, Restoris MCK Knee System, prosthesis, knee,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Apr 14, 2021
CODMAN HAKIM BACTISEAL Shunt System Clear with Barium Stripe Peritoneal Catheter 120cm, with drainage Holes and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Sabra Dipping Co, Classic Hummus ,10oz. PET cup, sealed with lid, 12 ct. Manufacturing Codes 300067. Expiration date…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sabra Dipping Company, LLC
FDA (openFDA food enforcement)
Reported Apr 14, 2021
Alaris Infusion Pump Module, Model 8100, serviced/repaired by Tenacor with an impacted bezel repair part
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tenacore LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Quaker Rice Crisps Sweet Barbecue Flavor, 3.03 oz. bag, UPC 0 30000 31984 0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Quaker Oats Company
FDA (openFDA food enforcement)
Reported Apr 7, 2021
BIOCARE Medical , IntelliPath FLX, Automated Staining Instrument, Ref: " Model Number:IPS0001US and IPS0001INTL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biocare Medical, LLC
FDA (openFDA device enforcement)
Reported Apr 7, 2021
ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually packaged femoral, tibial and patellar components…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 7, 2021
Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hollister Incorporated
FDA (openFDA device enforcement)
Reported Apr 7, 2021
Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Mar 31, 2021
BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm, XX.Xcm, XXg x XXcm REF XXXXXXX Note - for definition of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Mar 31, 2021
CAIRE DIAGNOSTICS FenomPro REF 900-0001 SN ***** - Product Usage: a portable, non-invasive device to measure fractional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Caire Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Mar 31, 2021
In-View Clear Leggings Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 31, 2021
Operating Table System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Group Logistics America, LLC
FDA (openFDA device enforcement)
Reported Mar 31, 2021
Mizuho CE IPX4, mode MOT-5602BW, 100-240, 50-60Hz, 400VA, REF 18-140-20 containing hand control Unit - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizuho OSI
FDA (openFDA device enforcement)
Reported Mar 31, 2021
Duodenoscope and accessories, flexible/rigid - Product Usage: used with an Olympus video system center, light source,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Mar 31, 2021
S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502 Components that are affected…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Communications
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.