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.

Medical devices

Reported Dec 30, 2020

APEX Compounding System Control Panel Module, REF: 601224, Product Code AX1000 - Product Usage: intended for…

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

B Braun Medical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

MicroScan Pos MIC Panel Type 34 - Product Usage: For the determination of antimicrobial agent susceptibility and/or…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Flexor Check-Flo Introducer, RPN KCFW-4.0-35-55-RB-HFANL0-HC, Order Number G56229 Flexor Introducers and Guiding…

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

Cook Inc.

20 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

42 IN (107 cm) Appx 5.0 ml, 20 Drop Admin Set, Spiros, REF: 20131-01; 31" (79 cm) Admin Set w/20 Drop Integrated Clave…

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

ICU Medical, Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)

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

Nova Ortho-Med Inc.

FDA (openFDA device enforcement)

Drugs

Reported Dec 23, 2020

CJC-1295, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

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

Advanced Nutriceuticals, LLC

16 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 23, 2020

BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of…

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

Carl Zeiss Meditec AG

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Percept PC Implantable Neurostimulator (INS) - Product Usage: The Percept PC is a neurostimulation device for deep…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Microsurgical Operating Room Tables;7300B (18-350-70);

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

Mizuho America, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in ablating a channel in occlusive peripheral vascular…

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

Ra Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Dec 23, 2020

+Protec Hands Antibacterial Gel Topical Solution Instant Sanitizer Hands 70% Alcohol Antiseptic, packaged in bottles of…

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

Simex Logistics SA de CV

4 more products in this recall

FDA (openFDA drug enforcement)

Meat & poultry

Reported Dec 19, 2020

FSIS Issues Public Health Alert for Ineligible Imported Raw Frozen New Orleans - Roasted Chicken Wings from the Peoples…

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

Fsis

USDA FSIS

Medical devices

Reported Dec 16, 2020

CORFLO NG/NI Pediatric Neonatal Feeding Tube w/ Anti-IV Connector

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

Avanos Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Usage: intended as a complete process control for…

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

3PLUS1 Multilevel Plasma Calibrator Set, Order No. 75128 - Product Usage: The kit is intended for amino acid metabolic…

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

Chromsystems Instruments & Chemicals GmbH

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

MAC VU360, Electrocardiograph

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

Shimadzu Mobile X-Ray System, MobileDaRt Evolution (MX8 Version), with adjustable handle option, Made in Japan -…

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

Shimadzu Medical Systems

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…

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

Spacelabs Healthcare, Ltd.

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2020

HomeChef Meal kit:One-Sheet Pretzel-Crusted Chicken with roasted broccoli and honey mustard..31.0 OZ (1 LB 15 OZ) 879g

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

The Kroger Co.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 16, 2020

PROKERA, non-sterile - Product Usage: Biologic corneal bandage.

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

TissueTech, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.…

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

Welch Allyn, Inc/mortara

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.