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.

Food

Reported Aug 29, 2018

Graeter's HANDCRAFTED French Pot ICE CREAM, Limited Edition KEY LIME PIE**ONE PINT (473 ml)**Nutrition Facts**GLUTEN…

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

Graeters Manufacturing Company

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

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

Handicare USA Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend, Net Wt. 15 lbs (6 / 2.5 lb bags per case), UPC…

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

J R Simplot Co. Corporate HQ

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12…

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

Johnson & Johnson Vision Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or…

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

Liebel-Flarsheim Company LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System Model#: 01EQ1000

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

O-Two Medical Technologies, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

Pasta Spinach with Cavatappi, Reser's Fine Food, item # 71117.14163, 2/4.5 # packages. UPC 0 71117 14163 4. Product is…

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

Reser's Fine Foods, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 29, 2018

Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3…

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

Salt & Straw LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

The Tri-Flo Subglottic Suction System

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

Vyaire Medical

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Connecting Bolt, Model 14-442093

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

Zimmer Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 23, 2018

Cargill Meat Solutions Retira Los Productos De Carne Molida Debido A Posible Contaminacin De E. coli O157:H7

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

Cargill Meat Solutions

USDA FSIS

Medical devices

Reported Aug 22, 2018

HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use only with Arrow One-Piece Percutaneous Sheath…

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

Arrow International Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

Hamilton-C1 Ventilator Unit Product Usage: The HAMILTON-C1 ventilator is intended to provide positive pressure…

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

Hamilton Medical AG

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Application (PKA) for use with…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body.

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

Merit Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 22, 2018

Sunny Side Farms Peanut Butter Cup Ice Cream; 48 oz. carton, 1.5 QTS (1.42L) UPC: 7-17544-20740 5 Allergens for Peanut…

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

Super Store Industries-Turlock Dairy Division

FDA (openFDA food enforcement)

Medical devices

Reported Aug 22, 2018

CDI Blood parameter monitoring system 500 H/SAT, Part No. 145883 Product Usage: The CDI System 500 provides continuous,…

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

Terumo Cardiovascular Systems Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Aug 22, 2018

alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free spf 50+ , 85 g 3 oz tube. Manufactured by: The Haine…

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

The Hain Celestial Group, Inc. - Worldwide HQ

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 22, 2018

ARCOS Modular Revision Hip System, item number 11-300814 orthopedic hip prosthesis femoral stem.

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

Zimmer Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

Slit Knife 2.6mm 45degree Bevel Up, Model Number 373726. for use in ophthalmic surgery.

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

Beaver Visitec

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

119" Blood Set w/200 Micron Filter, Clave¿, Rotating Luer, Sterile The blood tubing accessory with CLAVE Connector is a…

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

ICU Medical, Inc.

52 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Aug 15, 2018

Emergency First Aid Eyewash (Purified Water 98.3%), packaged in a) 4fl oz. (118 ml) NDC 7110500002, and b) 0.67 fl (20…

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

Longbow First Aid Products Manufactory

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 15, 2018

Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video…

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

Natus Neurology dba Excel Tech., Ltd. (XLTEK)

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.