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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 48,123 notices were distributed nationwide, so they reach California too — those are in the archive.

Medical devices

Reported Dec 25, 2019

Elasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Sterile. UPC 45713-58000 Bacteriostatic

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

Southwest Technologies Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2019

Vegetable eggroll 2 oz. and 3 oz.

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

T & R Enterprises USA, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 18, 2019

Habib EUS RFA, 10mm electrode active tip, Material Number/UPN: 6500 - Product Usage: The Habib EUS RFA is indicated for…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

CrossCath Support Catheter, RPN CXC3.0-1.9-14-90-P-NS-0, Order Number G51572 For diagnostic and interventional vascular…

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

Cook Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Coated PGA Undyed Polyglycolic Acid Braided Absorbable Suture Sterile EO 18" (45cm); UDI: (01)10790986000657 (17)220430…

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

CP Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Healix Knotless ADV BR 4.75 Suture Anchor

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

DePuy Mitek, Inc., a Johnson & Johnson Co.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2019

Lalamilo Farms Tropical Dreams Hawaiian Ice Cream - Strawberry Cheesecake. Sold in 3 gallon tubs, 1.5 gallon tubs, 5 L…

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

Edney and Sellers, Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 18, 2019

EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096

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

Encore Medical, LP

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2019

Terra Alba Calcium Sulfate Dihydrate packaged in 50 lb. bags; 25 lb. bags; 800kg (1764 lb.) bulk bags; 2000 lb. bulk…

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

Harrison Gypsum, LLC

FDA (openFDA food enforcement)

Food

Reported Dec 18, 2019

House Foods Chinese Mabo Tofu Sauce, mild; NET WT. 5.29 oz. (150 g) 4 servings UPC: 0 77377 74064 8 Ingredients: Water,…

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

House Foods America Corporation

FDA (openFDA food enforcement)

Meat & poultry

Reported Dec 18, 2019

Montpak International Inc. Retira Productos De Ternera Y Cordero Producidos Sin El Beneficio De Inspección De…

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

Recalling firm not stated

USDA FSIS

Medical devices

Reported Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

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

Integra LifeSciences Corp.

41 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943

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

Medtronic Navigation, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2019

Honey Mama s Truffle Bar (Trader Joe's) is a honey cocoa bar, refrigerated, one bar is packaged in flexible film, flow…

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

Nectar Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 18, 2019

P28, Titan 3-D Wedge, Evans, Large, 10 mm, sterile, REF P03-EVN-1010-S, Type: Lagrge, Size: 10mm, (01) 00889795018182,…

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

Paragon 28, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Dec 18, 2019

Ranitidine Tablets, USP 150 mg, OTC, a.) 30 count bottle (NDC 68788-7078-03), b.) 60 count bottle (NDC 68788-7078-06),…

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

Preferred Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 18, 2019

Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive Protein Reagent is intended for the…

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

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

MRIdian Linac Radiation Therapy System Model 10000 and 20000

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

Viewray, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 11, 2019

XEN Gel Stent, REF 5513-001(US Model), Sterile, RX Only, (01)10888628032439 ; Other Model Numbers: 5507-001(Global…

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

Allergan PLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 11, 2019

Quantam 2000 Electrosurgical Generator, Part number 909075.

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

CooperSurgical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 11, 2019

Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter, organic flour, organic sugar, organic eggs,…

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

Frog Hollow Farm

FDA (openFDA food enforcement)

Food

Reported Dec 11, 2019

Nat Cashew Flavor Type, 11.34 kg in each 4.2 gallon blue HDPE jerri-can, UPC: 20355428593

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

Givaudan Flavours Corp.

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 11, 2019

Hummingbird Wholesale Organic Chia Seeds, SD120-5#, packaged in a clear plastic bag with a while label, net wt. 5 lbs.…

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

Honey Heaven Wholesale Inc.

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.