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 22, 2025

CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, Plus 4-Way Stopcock…

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

Baxter Healthcare Corporation

15 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 22, 2025

Free Range Grade A Large Brown Eggs, 12ct Cartons, UPC: 860010568507, Black Sheep Egg Company 400 S Memorial Drive…

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

Black Sheep Egg Company, LLC

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 22, 2025

Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP…

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

Contego Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

DuoDERM" Extra Thin dressings are highly flexible, control gel formula dressings designed for use on dry to lightly…

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

ConvaTec, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

Zenith Alpha 2 Thoracic Endovascular Graft, Catalog Prefix ZTA2- Reference Part Numbers ZTA2-P-40-117-W ZTA2-P-40-167…

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

Cook Medical Incorporated

FDA (openFDA device enforcement)

Food

Reported Oct 22, 2025

Haifa COLD SMOKED SALMON 8 OZ.

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

D & M Smoked Fish, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 22, 2025

FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE IN GROUND TRANSPORTATION AMBULANCES.

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

Ferno-Washington Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US, used with Disinfection Kit User Manual, REF: UI-185043723

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

Fisher & Paykel Healthcare, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300. Product Description: The CycloPen…

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

Iantrek Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software…

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

Kico Knee Innovation Company

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

XERF EFFECTOR 60. Electrosurgical unit.

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

Lutronic Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED4528, FRED4026, FRED5526, FRED4508,…

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

Microvention Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 22, 2025

Fruit Cocktail IN 100% JUICE WITH ADDED INGREDIENTS; NET WT 15 OZ (425 g); Ingredients: Diced Peaches, Diced Pears,…

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

Pacific Coast Producers

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 22, 2025

Cardiac Workstation 5000; Model Number: 860439;

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

Philips North America

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 22, 2025

Sea Port brand, Raw Frozen Easy Peel Headless Shell-On White Shrimp, Jumbo size 16-20. Product of Indonesia.…

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

Sea Port Products Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 22, 2025

Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0895-01…

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

Spacelabs Healthcare, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 22, 2025

6+ Months SPROUT ORGANICS Made With Organic Sweet Potato, Apple & Spinach NET WT. 3.5 OZ (99g) INGREDIENTS: ORGANIC…

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

Sprout Organics Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 15, 2025

PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tuohy Epidural Needle - Winged and…

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

B Braun Medical Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 15, 2025

CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m

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

Corneat Vision, Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 15, 2025

o Nagatoshi Large AA Brown Omega-3 1 dozen cartons o Nijiya Large AA Brown Golden Yolk 1 dozen cartons o Mizuho Large…

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

Country Eggs, LLC

FDA (openFDA food enforcement)

Food

Reported Oct 15, 2025

Scott & Jon s Honey Sesame Salmon Rice Bowl

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

Demers Food Group LLC

FDA (openFDA food enforcement)

Food

Reported Oct 15, 2025

Taproom Gourmet brand 20lb and 18lb bulk "Fifth Avenue" Mix

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

Egress Capital Partners Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 15, 2025

FDR Visionary Suite, CH-200 Model/Version Numbers: (1) 566-16130-23, (2) 566-16130-31, (3) 566-16130-33

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

FUJIFILM Healthcare Americas Corporation

FDA (openFDA device enforcement)

Food

Reported Oct 15, 2025

G&L Food Dried Bean Curd Net WT 17.6 OZ (500G) INGREDIENTS: Soybean, Water, Magnesium Chloride as Preservative…

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

Gansu Zhaofeng Agricultural Development Co., Ltd.

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.