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.

Food

Reported May 21, 2025

Dixit Foods, Sabudana Khichadi, Net Wt. 200 g, Ingredients: Sago (Sabudana), Crushed Groundnuts, Sugar, DesiGhee, Salt,…

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

Bondsforever, Inc. dba Shastha Foods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 21, 2025

CMS8000 Patient Monitor

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

Contec Medical Systems Co., Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported May 21, 2025

LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported May 21, 2025

Beijing Soybean Paste, packaged in 8.82 ounce/250g red and white packages; Ingredients Soybean, Flour, Salt, Water,…

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

May Flower International Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 21, 2025

Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3010 Product Description: Contour…

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

Meddev Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 21, 2025

MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in…

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

Nipro Renal Soultions USA, Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 14, 2025

Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US

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

Ambu Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 14, 2025

Artix MT Thrombectomy Device, REF: 32-102

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

Inari Medical - Oak Canyon

FDA (openFDA device enforcement)

Food

Reported May 14, 2025

Ankimo branded Monkfish Liver; NET WT. 7 OZ (200g); Imported and DIST. BY: JJWV Marketing Corporation; Santa Fe…

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

JJWV Marketing Corporation

FDA (openFDA food enforcement)

Medical devices

Reported May 14, 2025

Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi…

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 14, 2025

Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported May 7, 2025

DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 7, 2025

Hyperthermia Pump Procedure Kit. Model Number: 902-00045. Sterile, single-use, disposable set used with the…

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

Belmont Instrument LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 7, 2025

Outer carton labeled: "Cookie Butter Banana Pie" Inner carton labeled: "Tropical Key Lime Pie" Product contained…

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

Dianne's Fine Desserts

FDA (openFDA food enforcement)

Medical devices

Reported May 7, 2025

HistoCore PELORIS 3, Model/Catalog Number: 45.0005/45.7512.501 A11, Software Version: 3.4.0. The HistoCore PELORIS 3…

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

Leica Biosystems Melbourne Pty Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported May 7, 2025

Enhanced Verify Evaluation Handset (CFN HH90130FA)

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Food

Reported May 7, 2025

La Victoria Cilantro Salsa; Med; Net Wt 15.5 OZ; UPC# 0 72101 34470 3; Distributed by: Megamex Foods, LLC Orange, CA…

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

MegaMex Foods LLC

FDA (openFDA food enforcement)

Drugs

Reported May 7, 2025

Dexonto 0.4% (dexamethasone sodium phosphate) solution 20 mg/5 mL (4 mg/mL), Rx Only, 12 - 5 mL Single Dose Units per…

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

Nubratori, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported May 7, 2025

Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Numbers:…

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported May 7, 2025

Stratus CS Acute Care cTNI TestPak.IVD test for cardiac troponin I in heparinized plasma.

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

Siemens Healthcare Diagnostics Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 7, 2025

Brand Name: Quantum Informatics - VIPER Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or…

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

Spectrum Medical Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 7, 2025

Ancient Grains Hoagie Roll, 4 oz, Paper carton (corrugated), CP45, Frozen

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

Upper Crust Bakery LP

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 7, 2025

Distal Femoral Augment; Item Numbers: (1) 880-300/11 (Sz. 0 - cemented sm), (2) 880-300/21 (Sz. 0 - cemented lg), (3)…

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

Waldemar Link GmbH & Co. KG (Mfg Site)

3 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported May 2, 2025

Ferrarini USA, Inc., Recalls Ready-to-Eat Prosciutto Products Imported Without Benefit of Import Reinspection

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

Ferrarini USA, Inc.,

USDA FSIS

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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.