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.

7,507 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.

Medical devices

Reported Sep 21, 2022

QIAcube Connect MDx, Model No. 9003070

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

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Steris Corporation Hopkins Facility

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per package, sterile.

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

Technomed Europe

FDA (openFDA device enforcement)

Food

Reported Sep 21, 2022

The GFB Gluten Free Bites Dark Chocolate and Coconut 1.2oz. UPC 856818008895, 10 retail units per tray, 6 trays per…

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

West Thomas Partners, LLC. dba Gluten Free Bar

FDA (openFDA food enforcement)

Medical devices

Reported Sep 14, 2022

Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In…

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

Abbott Molecular, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into…

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

Biosense Webster, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…

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

ICU Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN

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

OrthoPediatrics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea…

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

Philips Respironics, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 7, 2022

Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ.…

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

Family Dollar Stores, Llc.

5 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 7, 2022

T-SPOT.TB REF TB.300 US

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

Oxford Immunotec Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 7, 2022

Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice,…

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

Woodland Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2022

NUCLISENS easyMAG Magnetic Silica, REF 280133, 24 x 1.2mL bottles/kit.

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 31, 2022

Organic Amaranth Grain Gluten Free, Bob's Red Mill brand, packaged in Standup Pouch (24oz). Each case consists of 4/24…

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

Bob's Red Mill Natural Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2022

(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX;…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.

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

Intera Oncology, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…

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

Medtronic Neuromodulation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144

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

Mizuho OSI

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Nobel Biocare N1 TiUltra TCC NP 3.5x13mm

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

Nobel Biocare

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.

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

Wright Medical Technology, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 24, 2022

Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g) ready2eat Tomato paste,…

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

Albertsons Companies LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 24, 2022

(1) CVS Health Sterile Surgical Pads, Cushion Comfort, packaged 12 pads 5 in. x 9 in. per box, ASO Item No. 781083, SKU…

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

Aso LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 24, 2022

BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Food

Reported Aug 24, 2022

Whole Brown Almonds (bulk)

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

Blue Diamond Growers

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.