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 Dec 21, 2022

ARTISTE, ONCOR and PRIMUS with syngo RT Therapist with software version 4.3.1 MR3. Material Number: 8162815 Intended…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 21, 2022

Sardines in tomato sauce packed in cans labeled in part, "WILD PACIFIC SARDINES RAINCOAST TRADING TM***IN TOMATO…

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

St. Jean's Coast Mountain Resources Ltd. (dba) St. Jean's Ca

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

Small Joint OATS Set, REF AR-8981-06S, 6mm; and Small Joint OATS Set, REF AR-8981-08S, 8mm, both containing a…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors…

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

Bunnell, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit

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

Caire, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

Dewei DNA/RNA Preservation Kit, Catalog number DW-80005-1B

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

Dewei Medical Equipment Co. Ltd.

FDA (openFDA device enforcement)

Food

Reported Dec 14, 2022

Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC: 16430-69080 Keep refrigerated Product of Korea

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

Green Day Produce

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolumbosacral pedicle screw…

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

Integrity Implants Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044

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

Intersect ENT, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 14, 2022

Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per case

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

Nestle-USA, Inc. (Corporate Office)

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

The FAST System and the FAST PBC Prep Cartridge together are a closed, rapid and automated sample preparation system…

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

Qvella Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

IgA Immunoturbidimetric Assay- In vitro determination of IgA and IgM in serum and plasma Catalog Number: IA3832

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

Randox Laboratories Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic use with the IMMULITE and IMMULITE 1000…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

Accelerate PhenoTest BC kit REF 10101018

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

Accelerate Diagnostics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

Alcon Custom Pak Surgical Procedure Pack

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 7, 2022

Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz. individually wrapped plastic packages - 12 units per case UPC…

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

Amys Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 7, 2022

CMV IgM EIA, in vitro diagnostic.

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

Bio-Rad Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 7, 2022

Choi Heong Yuen Bakery Almond Cakes in round metal container Ingredients: mung bean powder (cereal containing gluten),…

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

fayeon distributors Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 7, 2022

GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel…

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

Greer Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200; BM-AD4K0200 BM-ADK0200 BM-CDK0200 BM-CFDK0200…

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

GS Biomark LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

INTUITIVE Da Vinci Xi 8mm SureForm 30 Curved-Tip Stapler Da Vinci Xi|X REF 488530 INTUITIVE Da Vinci 8mm SureForm 30…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 7, 2022

Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich 3 pk units - 8.75 oz (2.9 oz./unit) UPC: 8 5000988328 5…

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

Perfect Day Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 30, 2022

Tiramisu Twist Cookie 3.4 oz. packaged in a gold bag with a large image of two cookies on the package. SKU…

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

Daiso California Warehouse

FDA (openFDA food enforcement)

Medical devices

Reported Nov 30, 2022

Hamilton-C6

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

Hamilton Medical AG

FDA (openFDA device 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.