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.
Reported Nov 21, 2018
Chef Sensations Fire Roasted 1/2" diced onion/pepper blend Net Wt 20 lbs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Wornick Company
FDA (openFDA food enforcement)
Reported Nov 21, 2018
Affixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 17, 2018
Swift Beef Company Recalls Ground Beef Products due to Possible E. coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Swift Beef Company
USDA FSIS
Reported Nov 14, 2018
Inshell R/S 21/25 US-Select Pistachios NET WT. 25 lbs. 11.34 kg Product of the USA ARO Pistachio Inc. 19570 Avenue 88,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ARO Pistachios, Inc.
FDA (openFDA food enforcement)
Reported Nov 14, 2018
BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva Catheter), Catalog Number 383539 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2018
ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts Catalog Number: P2845B Dental Posts are implanted into…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coltene Whaledent Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2018
Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is intended to dilate stenoses in iliac, femoral,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Nov 14, 2018
Centricity PACS-IW with Universal Viewer version 5.0.x with PACS-IW foundation displays medical images (including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2018
FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Implants Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2018
Pointe Scientific AutoHDL/LDL Cholesterol Calibrator, Catalog Number H7545-CAL - Product Usage: For the calibration of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medtest Holdings, Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2018
REF VV19F Reinforced Dual Lumen Cannula, 19Fr., Sterile EO, DISPOSABLE: DO NOT RE-USE CE 0473 Product Usage: The OriGen…
High riskUsing this product could cause serious injury, illness or death — stop using it now.OriGen Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2018
VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Nov 14, 2018
TB Series Bipolar Pacing Leads, French Size 4F, 5F, 6F for Curve Type Straight, Atrial J, 60 degree Curve, and Right…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oscor, Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2018
EZ1 Advanced XL, Model Number: 9001492, GTIN: 04053228010760 Product Usage: The EZ1 Advanced XL is designed to perform…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
FDA (openFDA device enforcement)
Reported Nov 14, 2018
Simpurity HYDROGEL ABSORBENT SHEET WOUND DRESSING, 4" X 5", 10 Pads, Catalogue number SNS58315
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safe N Simple, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
3M Fast Release Varnish, 5% Sodium Fluoride, Mint Flavor, Rx Only, single use. 200 pack, with each package containing 1…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with supplements as a selective and…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Acumedia Manufacturers, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Posada Hatch Green Chile & Cheese Burrito, 72/4.5 oz burritos per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ajinomoto Windsor Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 7, 2018
Arrow AGB + Multi-Lumen CVC Kit, Cat. No. CDC-42703-B1A. Product Usage - The Arrow CVC is intended to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The battery housing is used to house the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2018
EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
BD Max Instrument Reader Spare Part, Catalog Number 8090369/443364, 44336409 (Repaired Reader spare part) - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Mushroom & Thyme Flatbread Pizza, Item 70610. Net Weight 7.65 lbs. 48-2.55 oz. portions. Keep Frozen. For institutional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Buddy's Kitchen Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 7, 2018
SOUTHWEST CRIMINI STUFFED MUSHROOM; 7oz. Black Foam Over-wrapped Trays; Keep Refrigerated; UPC 0081851202683
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Caito Foods LLC.
6 more products in this recall
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.