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 Sep 25, 2024

TxHA PEEK IBF/TxTiHA IBF System REF BTA-151 i. TxHA The Innovasis TxHA PEEK IBF System is an intervertebral body fusion…

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

Innovasis, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2024

ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is a mechanical thrombectomy device…

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

Microvention Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2024

HAWK Warming Grid, Item Number: 59-300

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

Safeguard US Operating LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 25, 2024

Bliss Tree Ragi Butter Murukku 200g UPC:8906087451754. Packaged in a box, 13 boxes per case Bliss Tree Ragi Butter…

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

Sri Lakshmi Narasimhar Overseas

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 25, 2024

VariSoft Infusion Set, Single Use.

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

Unomedical A/S

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2024

American Outdoor Products - Astronaut Strawberries, packaged in 0.5oz (14g) metallic plastic pouches. Sold individually…

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

American Outdoor Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2024

Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U

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

B Braun Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2024

FILMARRAY 2.0 INSTRUMENT, REF: FLM2-ASY-0001, FLM2-ASY-0001-W

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

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2024

Yummy Monkey Organics Butter & Yeast Popcorn, Made With Purified Ghee & Nutritional Yeast. UPC 9 96692 66641 2,…

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

Kester Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 18, 2024

BDAY CAKE MOCHI CRUNCH packed in pink plastic pouch packaging, net wt. 5oz, UPC 7189147148, Orwaiian LLC, 465 NE…

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

Orwaiian LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2024

Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP); Siemens Material Number (SMN): 11097543

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

Siemens Healthcare Diagnostics, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2024

NEUROSIGN Disposable Stimulating Dissector, REF 5888-00

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

Technomed Europe

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2024

Brand Name: Vit-l-escence Product Name: Vit-l-escence Singles A3 Model/Catalog Number: 1203- Software Version: N/A…

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

Ultradent Products, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2024

BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 11, 2024

Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per paper carton

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

MAMTAKIM, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 11, 2024

Sevoflurane E_Vap.(Quik-Fil):used with the A9 Anesthesia System-Used to provide the vapor of an anesthetic agent with…

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

Mindray DS USA, Inc. dba Mindray North America

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 11, 2024

Item 41303.82013, Reser's Essential Everyday Original Potato Salad, refrigerated product, net wt. 16oz. There are 6…

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

Reser's Fine Foods, Inc.

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 11, 2024

Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States:…

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

W L Gore & Associates, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2024

FreeStyle Libre 3 Sensors, REF: 72081-01, component of the FreeStyle Libre 3 Continuous Glucose Monitoring System

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

Abbott Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2024

DR 800. Digital Radiography X-ray System.

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

Agfa N.V.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2024

DxI 9000 Access Immunoassay Analyzer, Catalog #C11137.

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2024

Ion Endoluminal System, REF: 380748-65

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 4, 2024

Yummy brand Swirly Ices Tropical Tornado flavor Net Wt. 2.3 ounces (65g)x 8 popsicles, Total Net Wt. 18.34 ounces…

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

Paradise Distributors, LLC

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 4, 2024

CVS Health brand and HEB Baby brand Premium Infant Formula with Iron Milk-Based Powder; packaged in 964g composite…

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

PBM Nutritionals, LLC

FDA (openFDA food 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.