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.
Reported May 2, 2018
Oncomine Dx Target Test, (Model No. A32451), Oncomine Dx Target RNA/DNA Panel (Model No. A32441). A qualitative In…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
FDA (openFDA device enforcement)
Reported May 2, 2018
Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sofradim Production
FDA (openFDA device enforcement)
Reported May 2, 2018
Decorated (iced holiday cookies sold from self service cookie displays - cookies in the shape of eggs, bunnies and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Divinity Product Distribution LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Buenas Grated coconut - frozen; Kinayod na Niyog Noix de Coco Rape; UPC: 4806514650443 Keep Frozen Net Wt. 16 oz.,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Global Commodities Corp.
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Stage-1 Tissue Punch, Disposable, 4.5mm; catalog number: ISS141K. Intended for use in partially or fully edentulous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
FDA (openFDA device enforcement)
Reported Apr 25, 2018
Human Fetal Hemoglobin (HBF-1) FITC Conjugate
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
FDA (openFDA device enforcement)
Reported Apr 25, 2018
Cali Green Malay Kratom all packages, all quantities
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nutrizone LLC
9 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 25, 2018
SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10514 8
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Smucker Natural Foods, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Europe Ltd.
FDA (openFDA device enforcement)
Reported Apr 25, 2018
HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The J.M. Smucker Company, Inc.
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Amaranth Flour, Organic Whole Grain, Item Number: 6001C224, Net wt. 22 oz. UPC 0 39978 00911 1. The label is read in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bob's Red Mill Natural Foods, Inc.
FDA (openFDA food enforcement)
Reported Apr 18, 2018
First aid/emergency kits containing Honeywell eyewash: CSM kit number Kit/cabinet Description CSM Eyewash# Size:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Certified Safety Mfg Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
VOLISTA StandOP Surgical Light; Model numbers VLT600 SF AIM STP, VLT600 DF AIM STP, Ref. codes ARD568811901,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge US Sales LLC
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 18, 2018
6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear, NanoClave¿ T-Connector, Clamp, Rotating Luer, Bulk…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Hematology Diluent M-30D used with BC-3200 and BC-3600 Hematology Analyzer; Part Numbers: (1) 105-005405-00 (2 x 5.5L…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Spinal Jaxx Interbody Fusion Device, Model: 100001-511, Size: 9 H x 10 W x 25 L Product Usage: The Spinal Jaxx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neuropro Spinal Jaxx
FDA (openFDA device enforcement)
Reported Apr 18, 2018
AUTO REF/KERATOMETER ARK-1s
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical device, as part of system to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reliance Medical Products Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Magstim Company Limited
FDA (openFDA device enforcement)
Reported Apr 11, 2018
HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
2 more products 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.