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 Nov 6, 2024

Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor, 0.9m Model 809030006 Disp. SpO2 Forehead Probe, Adult,…

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

Nihon Kohden America Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to…

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

Percussionaire Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

Item 407118, UPC 13454 38493, Bistro 28 Creamy Green Chile Chicken Enchilada Express Meal Kit. Make 6 Enchiladas. Ready…

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

Reser's Fine Foods, Inc.

17 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 6, 2024

Sprouts Chicken Street Taco, 6 taco, perishable item kept under refrigeration, packaged in a plastic tray with plastic…

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

Sprouts Farmers Market

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2024

Brand Name: Vial2Bag Advanced¿ Product Name: Vial2Bag Advanced¿ 20mm Admixture Device Model/Catalog Number: 6070030…

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

West Pharmaceutical Services AZ, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

1) Flex Extenders, 5.2" x 15mm OD x 15mm ID REF S6411P 2) Flex Extender, 5.2" x 15mm OD x 22/15mm ID REF 7 5132 The…

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

Westmed, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

The outer package of the recalled product, Shirakiku Korean Seasoned Seaweed Korean Seaweed, is INCORRECTLY labeled as…

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

Wismettac Asian Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2024

AD-TECH Spencer Probe Depth Electrode, REF SD04R-AP58X-000 4-Contact 1.12mm (A style) Depth Electrode

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

Ad-Tech Medical Instrument Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2024

Principal Display: SureLife Foods PALEO BARS, Net Wt. 14 oz. (392 g.)- 14 ct. individually wrapped bars (28 g. each)…

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

Best Express Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2024

Boston Scientific myLUX Patient Application for an Apple Mobile device, Model Number 2939, Version 2.0.101, 2.0.110,…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2024

Soltive Premium SuperPulsed Laser - Intended for incision, excision, resection, ablation, coagulation, hemostasis, and…

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

Olympus Corporation of the Americas

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2024

STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP20 STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP15…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2024

Quantum Perfusion Systems for CPB, Roller Pumps use peristaltic action to propel blood through the venous and arterial…

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

Spectrum Medical Ltd.

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2024

Happy Moose Juice Tropical Roots packaged in a plastic 12 fl. oz. bottle. Ingredients: Mandarin Orange, Organic Carrot…

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

Youngstown Grape Distributors, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Meat & poultry

Reported Oct 24, 2024

FSIS Issues Public Health Alert for Ineligible Meat and Poultry Products Illegally Imported from the Republic of the…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Fsis

USDA FSIS

Medical devices

Reported Oct 23, 2024

IMMAGE Immunochemistry Systems IGM Immunoglobulin M Reagent REF 447610 IGM reagent, when used in conjunction with…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2024

KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco…

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

Kinova Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2024

Monarch Inflation Device 30 atm/bar REF IN2130 Injector And Syringe, Angiographic/Syringe, Balloon Inflation - The 30…

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

Merit Medical Systems, Inc.

15 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2024

Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR BLUE Model/Catalog Number: 4329BL Product Description:…

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

Nova Ortho-Med Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 23, 2024

S'mores Bites, 1 yummy pound, Distributed by Nuts.com, Cranford, NJ, 07016

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

Nuts.com

FDA (openFDA food enforcement)

Medical devices

Reported Oct 23, 2024

Cortera Spinal Fixation System Screw, Poly, Solid, 6.5mm x 45mm, REF: 150100-65045

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

XTANT Medical Holdings, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2024

Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005-01R. Monarch Platform (Bronchoscopy), REF: MON-000006,…

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

Auris Health Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 16, 2024

7-Eleven Fudge Brownie with Chocolate Chip, 3.5 oz. UPC: 05254856392

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

Innovation Bakers, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 16, 2024

MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing W/APPLICATOR, 1.5oz tube (Model Number 31515)…

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

Integra LifeSciences Corp.

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.