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 Feb 8, 2023

OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental…

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

Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Feb 8, 2023

Conzerol zero molluscum contagiosum, Homeopathic treatment for Molluscum Contagiosum, Topical Cream, Net weight 0.78 oz…

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

Discovery Pharma LLC

FDA (openFDA drug enforcement)

Meat & poultry

Reported Feb 8, 2023

FSIS Issues Public Health Alert for Ready-To-Eat Pork Sausage Products Due to Misbranding and an Undeclared Allergen

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Goulart's Sausage Co.

USDA FSIS

Medical devices

Reported Feb 8, 2023

AxiEM" Non-Invasive Patient Tracker

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 8, 2023

Limited Edition Winter Mint Chocolate Premier Protein 30g Protein High Protein Shake 11.5oz (340mL) UPC 00643843801498…

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

Niagara Bottling

FDA (openFDA food enforcement)

Medical devices

Reported Feb 8, 2023

Lucid TCD 2.0 System, Model: NA-LUCM1. Transcranial Ultrasound System

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

NovaSignal Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 8, 2023

CADD Administration Set, List Numbers: a) REF 21-7346-24; b) REF 21-7363-24

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

Smiths Medical ASD Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 8, 2023

SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000

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

SynCardia Systems LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 8, 2023

Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized by a…

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

Turbett Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 8, 2023

Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 20 TESTS/1 KIT Green…

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

Universal Meditech Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 8, 2023

GORE CARDIOFORM Septal Occluder, REF: GSX0030A

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

W L Gore & Associates, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

Invisalign Express 10 REF 8512 Invisalign System Comprehensive REF 9000 Invisalign System Moderate REF 9001

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

Align Technology Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

biokitHSV-2 Rapid Test, REF: 300028001

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

Biokit, S.A.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use.

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

CooperVision, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

Future Diagnostics STAT-IntraOperative-Intact-PTH (STAT-IO-I-PTH) Immunoassay kit REF 4K-IPT-00. in vitro diagnostic.

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

Future Diagnostics Solutions B.V.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

Getinge Flow-i Anesthesia Systems Flow-i C20, Part no. 6677200 Flow-i C30, Part no. 6677300 Flow-i C40, Part no. 6677400

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

Getinge USA Sales Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

Revogene SARS-CoV-2_IVD real-time RT-PCR test intended for the qualitative detection of RNA from SARSCoV-2 Catalog…

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

Meridian Bioscience Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

Air-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Size REF Number 0.0 50005 0.5 50055 1.0 50105 1.5 50155 2.0…

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

SunMed Holdings, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation

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

Teleflex LLC

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jan 25, 2023

Rasagiline Mesylate Tablets 1 mg; 30 tablets in HDPE bottle; Rx only; NDC 67877-260-30; Manufactured by Alkem…

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

Ascend Laboratories, LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 25, 2023

R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control, REF 3D501, containing 10 x 2.0mL Control N;…

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

R & D Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2023

BD Pyxis MedBank System - Product Label/labeling pending

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2023

TOHATO Nagewa Snack Salty Taste 27g and 73g units UPC numbers: 4901940112036 & 4901940112005 Product sold individually,…

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

Daiso California Warehouse

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2023

Codman Surgical Patties, Part number 801400; SURG PATXRAY 1/2X1/2-200; Lot 6396457

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

Integra LifeSciences Corp.

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.