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 May 22, 2024

Patient Information Center iX and Patient Information Center iX Expand, Software Version 4.x.

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

Philips North America LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2024

TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm,…

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

TriMed Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2024

GE Healthcare Innova IGS 5, computed tomography x-ray system

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

GE Medical Systems, SCS

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 15, 2024

Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsule dietary supplement, Folate 1667mcg DFE, 5000mcg Folic Acid, 120…

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

HTO Nevada Inc. dba Kirkman

FDA (openFDA food enforcement)

Medical devices

Reported May 15, 2024

5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/795143, 5500 W/795144, 5500 G/795145, and…

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

Philips Ultrasound, Inc.

FDA (openFDA device enforcement)

Food

Reported May 15, 2024

Martinelli's Gold Medal Apple Juice From U.S. Grown Fresh Apples 1 Liter (33.8 fl oz.) No Additives of Any Kind UPC 0…

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

S Martinelli & Company

FDA (openFDA food enforcement)

Food

Reported May 15, 2024

Java Wafer - Mocha Hazelnut [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]

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

Sacramento Cookie Factory

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 15, 2024

PERLA TL 25D SCREW REF: TLF-DS 45 25-S TLF-DS 45 30-S TLF-DS 45 35-S TLF-DS 45 40-S TLF-DS 45 45-S TLF-DS 55 30-S…

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

Spineart Sa

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Abbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,

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

Allergan Sales, LLC

FDA (openFDA device enforcement)

Food

Reported May 8, 2024

Longreen Corporation 4 in1 Reishi Coffee, 18.2 grams/sachet, 10 sachets/box

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

BF Suma Pharmaceuticals, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 8, 2024

Medtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100, REF: PMAC71RIC

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

Covidien

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup

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

Innomed, Inc.

FDA (openFDA device enforcement)

Food

Reported May 8, 2024

International Bread Pita Chips Retail Clamshell Container: 10oz., Bulk bag: 10lbs. UPC: Plain Baked Pita Chips: 6 81942…

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

International Pita Bread, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 8, 2024

Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test Chamber 21 Gauge REF OPOHF21L The…

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

Johnson & Johnson Surgical Vision, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Galaxy System REF GAL-001 (specifically GAL-019, Wired Controller) The Galaxy System and its accessories are intended…

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

Noah Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

POWERSEAL 5 mm, 23 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such…

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

Olympus Corporation of the Americas

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Battery Mobile X-ray Unit EASY MOVING Model with telescopic column 3.1, model numbers: a. SM-20HF-Batt; b.…

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

Sedecal Sa

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly

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

Thoratec Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

3M Durapore Surgical Tape, Catalog Number 1538-118

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga Chang Hydrodissection Cannulas. These Custom…

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported May 1, 2024

Amy's Kitchen Enchilada Verde Whole Meal 10 oz. 12 pk Item # 000085

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

Amy's Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 1, 2024

Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and pelvic surgery

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.

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

Parker Laboratories, Inc.

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.