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.
7,515 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.
Reported Nov 28, 2018
Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merck Millipore Ltd.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
Organic green whole cardamom pods; 55.12 Pound bags; Product of Guatemala
High riskUsing this product could cause serious injury, illness or death — stop using it now.AMI Newco
FDA (openFDA food enforcement)
Reported Nov 21, 2018
OviTex Reinforced BioScaffold 4x8cm, Part Number F10254-0408G
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AROA Biosurgery, Ltd.
20 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
Arrow AGB+ Multi-Lumen CVC Kit, 7 Fr., 3 Lumen, 20cm catheter length, .025 inch dia. spring-wire guide, Product Code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
-Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME) Panel REF RFIT-ASY-0118 30 For FilmArray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Nov 21, 2018
bioM¿rieux NucliSENS easyMAG Lysis Buffer ref. 280134
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
ERBITUX CETUXIMAB Injection, 200 mg/100 mL (2 mg/mL), 100 mL per single-use vial, Rx only, Manufactured by: ImClone…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Eli Lilly & Co.
FDA (openFDA drug enforcement)
Reported Nov 21, 2018
Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml EMP160ECO-US-5 (GTIN:5060358120367) Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Espiner Medical Ltd.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Nov 21, 2018
MarieBelle brand Japanese Matcha Japanese Green Tea and White Chocolate Bar, NET Wt. 2.82 oz. UPC code: 877708005886
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maribel's Sweets, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 21, 2018
Progesterone SR 100 mg Capsules, packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Right Value Drug Stores, Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 21, 2018
Rojo's Autentico Black Bean 5 Layer Dip; Layers of Black Beans, Guacamole, Salsa, sour Cream and Cheddar Cheese. NET…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simply Fresh Foods, Inc.
FDA (openFDA food enforcement)
Reported Nov 21, 2018
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
simple truth organic Red Quinoa Ingredients: organic red quinoa Distributed by The Kroger Co, Cincinnati, OH…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Kroger Co.
FDA (openFDA food enforcement)
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)
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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.