All recall categories

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.

Medical devices

Reported Dec 5, 2018

PNEUMOCLEAR Heated High-Flow Tube Set Product Usage: The Heated High-Flow Tube Set is a single use sterile tube set…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

WOM World

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

Ascom Telligence Nurse Call System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ascom (US) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 28, 2018

Roasted Corn Salsa; Net Weight: 10 lbs. (10 x 1 lb. bags) Corner Bakery Caf¿ Brand Ingredients: Corn, Red Onion,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cadence Gourmet LLC

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 28, 2018

Recchiuti Bittersweet, Smooth, rich and complex. Net Wt. 3 oz. (85 G) Also sold in case of 12 UPC 8019895 00017 6…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Confections by Michael Recchiuti

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 28, 2018

HOUSE BLEND Barbecue SAUCE INGREDIENTS: ***Contains 2% or less of Soybean Oil***Onion Powder***Calcium Disodium…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Diamond Crystal Brands, Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 28, 2018

Signature Select Mexican Style Roasted Corn; 12 oz.; 12/12oz. units per case; Keep Frozen Until Ready To Use; UPC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Harvest Food Group

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 28, 2018

Irrisept OR, Finished Bottle Assembly 450 ml STEP 1

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

FDA (openFDA device enforcement)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Drugs

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Drugs

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)

Food

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)

Medical devices

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)

Food

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)

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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.