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 48,123 notices were distributed nationwide, so they reach California too — those are in the archive.

Medical devices

Reported Mar 25, 2020

IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use…

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2020

LEGION PS High Flex XLPE size 5-6 9mm Articular Insert

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2020

Rheumatoid Factor (RF) Kit for use on SPAPLUS, for in-vitro diagnostic use, Product code: LK151.S.A. , UDI:…

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

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Food

Reported Mar 25, 2020

Vita Wild Herring in Wine Sauce 32oz plastic jar, UPC 22635 40011, 6 jars per case Ready to Eat Keep Refrigerated

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

Vita Food Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2020

OsteoSelect Demineralized Bone Matrix (DBM) Putty 10.0cc in a syringe; STERILE R, Product Code: 359100, Dimensions:…

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

Xtant Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102…

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

ARJOHUNTLEIGH POLSKA Sp. z.o.o.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general…

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

Cardinal Health 200, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

BodyGuard Microset REF A120-003XYVA, Sterile EO, Tubing: 150 in. (380 cm), Prime Vol: approx. 8ml Product Usage: The…

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

CME America, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2020

Profile Food Ingredients, 10# Choc Dairy Pwd PFI-1010, packaged in 50 lb bags.

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

International Food Products Corporation

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 18, 2020

Sunny Select Au Jus Gravy Mix 1 OZ pouch (24 pouches per case)

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

McCormick & Company, Inc. - Flavor Manufacturing Center

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2020

Randox Laboratories Ltd. Catalogue Number CQ5052, Lot Number 4244CK (relabeled as Response Biomedical Catalogue Number…

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

Response Biomedical Corp.

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2020

Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato…

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

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Food

Reported Mar 18, 2020

American Bounty brand Icing Mix Vanilla, Item #32595, in 5 lb. metallic pouches, 6 pouches per case.

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

Tova Industries Inc.

21 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2020

GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

SoundWave Professional Suite Software 3.2, Ref CI-6055-014, SPN 058-023-32085, UDI: (01)07630016853227, Logical…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Advanced Bionics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Bard Biopsy EnCor Probe, Stereotactic/Ultrasound 7G, REF number ECP017G, packaged individually in sterile pouches, 5…

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

Bard Peripheral Vascular Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Enzymatic Creatinine Reagent (CR-E 2 X 200), REF A60298, For in Vitro Diagnostic Use, Rx Only, UDI: 15099590625733

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

Beckman Coulter Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 11, 2020

Blendtopia Superfood Smoothie Kit Glow flavor, 7 oz flexible pouch

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

Blendtopia Products, LLC

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 11, 2020

CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)

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

CareFusion 303, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 11, 2020

Aminature L-Cysteine HCl Anhydrous 100 mesh 25KG DRUM

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

Cj Haide (Ningbo) Biotech Co., Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 11, 2020

Monitor for the Functional Imaging System for Magnetic Resonance Imaging System

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Remisol Advance running on hardware with Windows XP, Windows 7, Windows Server 2003 and Windows Server 2008 operating…

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

Normand-Info S.A.S.U.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

RespVent Closed Suction System T-Piece Tracheostomy Adult, Diameter: 4.6mm (14F), Length: 30.5cm (12in.), MDI Adapter,…

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

Respiratory Therapeutics Group LLC

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.