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 48,100 notices were distributed nationwide, so they reach California too — those are in the archive.

Medical devices

Reported Oct 15, 2025

FlexLab (FLX) System. Potassium Test System. in vitro diagnostic

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

Inpeco S.A.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 15, 2025

Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with…

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

M.O.M Enterprises, LLC.

FDA (openFDA food enforcement)

Food

Reported Oct 15, 2025

COOKED LINGUINE PASTA 6 x 5 lb Net Wt. 30lbs (13.60kg) PERISHABLE KEEP FROZEN

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

Nate's Fine Foods, LLC

8 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 15, 2025

Toto S'Mores Ooey Gooey Cookie; Gluten Free & Dairy Free; Net Wt. 2.25 OZ Rear panel: Packed with superfoods; Gluten,…

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

Toto Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 8, 2025

Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to identify internal wiring anomalies in the…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

Change Healthcare Radiology Solutions software version 14.2.2

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

Change Healthcare Canada Company

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Product…

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

Draeger, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 8, 2025

Shrimp Cocktail Bowl; 7oz clear plastic retail packaging. UPC: 011110622952 Shrimp Cocktail Bowl; 17oz clear plastic…

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

Lawrence Wholesale LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 8, 2025

Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616, (2) AG 630, (3) AG 636, (4) AG 640, (5) AG 645, (6) AG…

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

LeMaitre Vascular, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: KIT, TCCC Training- Complete…

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

North American Rescue LLC.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-410-152. The NES Reprocessed…

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

Northeast Scientific Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

IMPLANT EPIKUT PLUS MT16 3,5X10,0MM, REF: ILM 3510N; IMPLANT EPIKUT PLUS MT16 3.8X11.5MM, REF: ILM 3511N; IMPLANT…

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

S.I.N. Implant System Ltda

FDA (openFDA device enforcement)

Food

Reported Oct 8, 2025

Frozen Raw Easy Peel shrimp, IQF, 2-lb bag, 10 bags/case; Generic Brown cardboard box UPC: 021130123223

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

Tas Tematic Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 8, 2025

GORE ACUSEAL Vascular Graft, REF: ECH050020J, ECH050020W, ECH050050J, ECH050050W, ECH060010A, ECH060020A, ECH060020J,…

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

W L Gore & Associates, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2025

Automated Impella Controller (AIC) with the below brands and product codes. Used with heart assist pump. 1. Impella…

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

Abiomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2025

FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative, multiplexed, nucleic acid-based in vitro diagnostic test…

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

Biofire Defense

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2025

Extractor Pro RX Retrieval Balloon Catheter; UPN (REF): (1) M00547030 (9-12mm Below), (2) M00547000 (9-12mm Above);

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Oct 1, 2025

PURE CANE GRANULATED SUGAR, NET WT 50 LB (22.67kg), Distributed by Domino Foods, Inc., Yonkers, NY 10705, STORE IN A…

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

Domino Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 1, 2025

STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device, SFX SPI PDS+ BI VIO 14X14IN(36X36CM) USP1(M4)…

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

Ethicon, LLC

FDA (openFDA device enforcement)

Food

Reported Oct 1, 2025

GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET WT 5.25 OZ (149g) INGREDIENTS: GOODLES SPIRALS…

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

Gooder Foods, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 1, 2025

Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION…

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

MEDLINE INDUSTRIES, LP - Northfield

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Oct 1, 2025

ARTISAN OF SKIN (Benzoyl Peroxide 10%) , 7 oz (201 g), Artisan of Skin Beverly Hills, CA 90210

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

Private Label Skin Care Inc.

5 more products in this recall

FDA (openFDA drug enforcement)

Food

Reported Oct 1, 2025

UDK ,Half Plum, 170 g, Container, 24, ambient

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

Sungal Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 24, 2025

Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number:…

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

Agilent Technologies Denmark ApS

2 more products in this recall

FDA (openFDA device enforcement)

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Other states

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.