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.
7,507 stored notices name California, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported Dec 7, 2022
CMV IgM EIA, in vitro diagnostic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2022
Choi Heong Yuen Bakery Almond Cakes in round metal container Ingredients: mung bean powder (cereal containing gluten),…
High riskUsing this product could cause serious injury, illness or death — stop using it now.fayeon distributors Inc.
FDA (openFDA food enforcement)
Reported Dec 7, 2022
GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greer Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 7, 2022
CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200; BM-AD4K0200 BM-ADK0200 BM-CDK0200 BM-CFDK0200…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GS Biomark LLC
FDA (openFDA device enforcement)
Reported Dec 7, 2022
INTUITIVE Da Vinci Xi 8mm SureForm 30 Curved-Tip Stapler Da Vinci Xi|X REF 488530 INTUITIVE Da Vinci 8mm SureForm 30…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2022
Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich 3 pk units - 8.75 oz (2.9 oz./unit) UPC: 8 5000988328 5…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Perfect Day Inc.
FDA (openFDA food enforcement)
Reported Nov 30, 2022
Tiramisu Twist Cookie 3.4 oz. packaged in a gold bag with a large image of two cookies on the package. SKU…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Daiso California Warehouse
FDA (openFDA food enforcement)
Reported Nov 30, 2022
Hamilton-C6
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical AG
FDA (openFDA device enforcement)
Reported Nov 30, 2022
K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kamiya Biomedical Company, LLC
FDA (openFDA device enforcement)
Reported Nov 30, 2022
PAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong Soft Catheter, Closed Tip, 19G, Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pajunk Medical Systems, LP
FDA (openFDA device enforcement)
Reported Nov 30, 2022
Nourish Inc. brand Fruit Snack Pack SNACK ATTACK 6.48 oz. Apples, Medjool Dates, Blackberries, Sunflower Butter Keep…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sodexo, dba Nourish
FDA (openFDA food enforcement)
Reported Nov 30, 2022
The Tomato Head Beet Hummus packaged in 8oz PPE plastic cups - 8 cups per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tomato Head Foods
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 23, 2022
Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 23, 2022
EasyStand Bantam, with the following sizes. a. Small; b. Extra Small. Used for assisting individual in standing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Altimate Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Hill-Rom Progressa Bed System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2022
125 series iGO2 Portable Oxygen Concentrator-indicated for the administration of supplemental oxygen. Models: 125D,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeVilbiss Healthcare LLC
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Extension Tabletop for Operating Table System 1140, Model Nos. 1140.20F0 and 1140.20AN
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER 10MM TIP product. Used to necrotize or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2022
OneLIF Torque Limiting Adapter, AO to 1/4 SQ, 2.25Nm Limit, Catalog #015-010-0000, a component of NovApproach Spine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novapproach Spine LLC
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Philips Laser System, REF: LAS-100. Used in minimally invasive interventional procedures within the cardiovascular…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
FDA (openFDA device enforcement)
Reported Nov 16, 2022
Disc Preparation instruments contained in the following products: CI-11050-08102515 Longer IdentiTi PO Trial Tip, 11A X…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2022
Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avanos Medical, Inc.
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.