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 Feb 6, 2019
Dakota Specialty Milling Enhanced Flax Flour Blend, 42205, Net Wt 50 lbs. Ground Flax, Calcium Sulfate, inulin, VM 112…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dakota Specialty Milling, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 6, 2019
Cell Saver 5/5+ Bowl Set, 70ml, Product ID: 0291E-00, 0291A-00 Indications for Use: The Haemonetics Cell Saver 5/5+…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haemonetics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 6, 2019
Peaches, sold as a bulk retail item, with PLU 4044, and country of origin of Chile. The peaches sold at Aldi are…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jac Vandenberg Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 6, 2019
Calix Lumbar Spinal Implant System: 22mm x 10mm x 7mm PLIF ASSY PC, REF X034-0172PC 22mm x 10mm x 8mm PLIF ASSY PC, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xtant Medical Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2019
Q's American Best Trading Inc. Recalls Siluriformes Products Produced Without Benefit of Import Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Q's American Best Trading Inc.
USDA FSIS
Reported Jan 30, 2019
Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned with Red & Green Peppers. NET WT 15.25 oz. (432 g);…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Research Center - Walnut Creek
FDA (openFDA food enforcement)
Reported Jan 30, 2019
VentStar Basic 180, Catalog Number MP00349 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 30, 2019
Perfusion Pack, Rx only, Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA
FDA (openFDA device enforcement)
Reported Jan 30, 2019
Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Product Code: PF2-WP33 Product Usage: The PRISMAFLO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stihler Electronic GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 30, 2019
BW Lasso 2515 ANV eco Variable Diagnostic EP Catheter, REF D134301 Diagnostic electrophysiology (EP) catheters are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Jan 23, 2019
Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Jan 23, 2019
PERMA-HAND Silk Suture Size 5, Black 30" (75cm) Double Armed LR Needles, Product Code 485T Product Usage: PERMA-HAND*…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported Jan 23, 2019
U by Kotex¿ Sleek¿, Regular Tampons, 18 Count
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 23, 2019
PREMIER Cryptococcal Antigen, Catalog Number 602096 Product Usage: The PREMIER Cryptococcal Antigen enzyme immunoassay…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2019
H & T Seafood, Inc. retira productos siluriformes producidos sin el beneficio de inspección de importación
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Jan 16, 2019
Adam Bros. Family Farms Red Leaf Lettuce 24 heads per carton Adams Bros Family Farms and Ovation
High riskUsing this product could cause serious injury, illness or death — stop using it now.Adam Bros. Farming, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 16, 2019
Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 16, 2019
Ingenia Elition S, Ingenia Elition X
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederlands
FDA (openFDA device enforcement)
Reported Jan 16, 2019
Siemens Biograph Horizon PET/CT System, Product Usage: The Siemens Biograph systems are combined X-Ray Computed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 9, 2019
StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 9, 2019
Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultradent Products, Inc.
FDA (openFDA device enforcement)
Reported Jan 2, 2019
Eat Smart Salad Shake Ups - Asian Sesame/Sesame Asiatique; 5.5 oz. (156 g); UPC 7 09351-30241 1, 7 09351 30244 2…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Apio, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 2, 2019
GEM Coupler Forceps, GEM4183C, packaged individually.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jan 2, 2019
Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit per Cavity #3 Cavity Deep/20 pieces per case…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, 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.