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 48,122 notices were distributed nationwide, so they reach California too — those are in the archive.

Medical devices

Reported Aug 5, 2020

Tube Set for TEM - Product Usage: Transanal Endoscopic Microsurgery (TEM) combination system and the instrument set for…

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

Richard Wolf GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2020

Computed Tomography X-ray System; Model uCT 760; Rx; UDI: (01) GTIN: 06971576831043 - Product Usage: intended to…

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

Shanghai United Imaging Healthcare Co., Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2020

Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device…

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

Teleflex Medical Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2020

Ablation Galil Technology, IcePearl 2.0 CX 90 Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation…

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

Boston Scientific Corporation

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2020

Thora-Para 5 Fr Non-Valved Catheter Drainage Tray

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

Carefusion 2200 Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 29, 2020

Red Velvet Layered Cheesecake is one whole cake (9" round cake) that has been pre-sliced into 14 slices and packaged in…

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

Chuckanut Bay Foods LLC

FDA (openFDA food enforcement)

Food

Reported Jul 29, 2020

Aminature L-Cysteine HCl Anhydrous 100 mesh 25KG DRUM

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

Cj Haide (Ningbo) Biotech Co., Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 29, 2020

Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal,…

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

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2020

Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended…

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

NuVasive Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2020

syngo.via RT Image Suite with software versions syngo.via VB30 or VB40

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2020

LoFric Origo, Nelaton, 16in, FR10 urinary catheters

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

Wellspect HealthCare (Division

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2020

BodyGuard BodySet, REF: A120-160SAS

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

CME America, LLC

36 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2020

This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product…

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

Djo, LLC

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2020

***KIND HEALTHY GRAINS***Oats & Honey Granola with Toasted Coconut***INGREDIENTS: Oats, tapioca syrup, brown rice, cane…

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

Kind LLC

FDA (openFDA food enforcement)

Food

Reported Jul 22, 2020

WinCo Foods Tater Bites Shaped, Shredded Potatoes, frozen product. Retail 32 oz. poly bag has UPC 0 70552 30303 4. The…

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

Lamb Weston Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 22, 2020

DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide…

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

Neocis Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2020

ACUMED CALLOS INJECT 10CC. Product Number: 65-0010-S, UDI: 813845020245 - Product Usage: Callos is indicated to fill…

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

Skeletal Kinetics, LLC

44 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2020

Whole Foods Market Red Velvet Layered Cheesecake Slice PLU: 78620 packaged in plastic clam shell with scale label…

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

Whole Foods Market

FDA (openFDA food enforcement)

Medical devices

Reported Jul 15, 2020

The CapsoCam Plus (SV-3); Device Common Name: System, Imaging, Gastrointestinal, Wireless, Capsule; Catalog Number 2795…

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

Capso Vision, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 15, 2020

FHC Guideline 4000 5.0 GL5 Main Processing Unit - Product Usage: intended to record and stimulate electrophysiological…

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

FHC, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 15, 2020

Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes. Sterile and single use only. Catalog number…

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

Kentec Medical, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 15, 2020

Extra corporeal circuit with bio-active surface.

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

Medtronic Perfusion Systems

FDA (openFDA device enforcement)

Medical devices

Reported Jul 15, 2020

EasyDiagnost Eleva DRF, model no. 706050 - Product Usage: X-ray system, diagnostic, general-purpose.

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

Philips North America, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 15, 2020

Blanxart 85% Nicaragua Organic Dark Chocolate Bar, packaged in paper packaging with internal foil wrapper. Net weight…

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

Power Selles Imports dba Culinary Collective

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.