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.

7,506 stored notices name California, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach California too — those are in the archive.

Food

Reported Feb 14, 2024

Ito-Shoten Seasoned Mushroom 200g/7.06 oz. Product of Japan Distributed by Mitsuwa Corporation Torrance, CA 90501

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

Mitsuwa Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Feb 14, 2024

Total immunoglobulin M (IgM total) IVD, kit, nephelometry/turbidimetry

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 7, 2024

MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL HLD STR JAW 220MM";

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

Aesculap Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 7, 2024

the original BENNY T'S VESTA DRY HOT SAUCE GHOST NET WT. 1.5OZ INGREDIENTS: Fresh Chilies, Onions, Breadcrumbs…

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

Benny Ts Vesta Inc. dba Vesta Firey Gourmet Toppings

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 7, 2024

Surgilon Braided Nylon sutures: 88861919-31 SURGILON* 4-0 BLK 7X75CMPCT 88861919-41 SURGILON* 3-0 BLK 7X75CMPCT…

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

Covidien LP

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 7, 2024

202225 SALMON BAKKA FROST FILLET 6/7KG FR FRO F LB 202002 SALMON BAKKAFROST FAROE ISLANDS 5/6KG FR FRO F LB 202012…

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

Ocean Group Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 7, 2024

EZDilate Fixed Wire Balloon 6-7-8. Indicated for endoscopic dilation of strictures of the esophagus in adults and…

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

Olympus Corporation of the Americas

11 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 7, 2024

Rizo Bros Cotija (Grated) 8 oz. UPC 72724200043 7 oz. UPC 7-27242-14022-5 Tio Francisco, Casa Cardenas 9 oz. UPC…

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

Rizo Lopez Foods, Inc. dba Don Francisco Cheese

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 7, 2024

NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code…

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

THOR Photomedicine Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 7, 2024

Volar Bearing Plate. REF: VBEAL-3-7N, VBEAL-5-7N, VBEAL-3-7S, VBEAL-5-7S, VBEAL-7-7S, VBEAL-3-7W, VBEAL-5-7W,…

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

TriMed Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 7, 2024

Melissa's Hot Kimchi Pickled Napa Cabbage NET WT. 14 oz (397g) Ingredients: Napa Cabbage, Radish, Water, Garlic, Red…

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

World Variety Produce Inc. dba Melissa's

FDA (openFDA food enforcement)

Medical devices

Reported Jan 31, 2024

Accure Laser System, Model: PFMS00004

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

Accure Acne, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

bkActiv Ultrasound System 2300, Model numbers 2300-56 and 2300-66.

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

B-K Medical A/S

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2024

DeIorio Foods, Inc. brand Cafe Pizza Dough Sheet; Keep Frozen

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

DeIorio Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 31, 2024

PANTHER FUSION System REF 9121010000 The Panther System is an integrated nucleic acid testing system which fully…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

Snapshot NIR, REF: KD204

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

Kent Imaging, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2024

R&B Chocolate Chips Croissant Twist

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

Lecoq Cuisine Corporation

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 31, 2024

Power Knee, REF: PKA10001, and PKA10003; with Power Knee Battery, REF: PKA10002

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

Ossur H / F

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an 8F distal section, Sterile.

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

St. Jude Medical, Atrial Fibrillation Division, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2024

Vermont Village Unsweetened Apple Sauce (24oz)

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

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 31, 2024

Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile.

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

Tornier, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 24, 2024

FreeStyle Libre 3 App, part of Continuous Glucose Monitoring System, when used on the Android 13 Operating System

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

Abbott Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 24, 2024

PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number…

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

Becton Dickinson & Company

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.