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.
7,507 stored notices name California, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported Jul 27, 2022
X80 RADiant Photoelectric Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xstrahl Limited
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Alcon Custom Pak Surgical Procedure Pack: 16998-11 2519351H SALAHUDDIN 2.4 PACK FRESNO SURGICAL HOSP 18392-03 14HDFF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Jul 20, 2022
PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis US Corp.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
HAMILTON-H900 Humidifier, Models: 950001, 950004
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hamilton Medical AG
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Invacare Platinum 5NXG Oxygen Concentrator, Model Numbers P5NXG1, P5NXGC1 (Canada specific model)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Favorite Day Lavender Shortbread Cookie Bites Net Wt 7oz (198g) packaged in a purple bag and an inside silver flexible…
High riskUsing this product could cause serious injury, illness or death — stop using it now.J & M Foods, Inc.
FDA (openFDA food enforcement)
Reported Jul 20, 2022
Market Day Krabbycakes, Item 3320, Net Wt. 40 oz. (2.5 lbs.) 1.13kg. Item Number 803320R. UPC 51497 14360. Light panko…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Market Day Local Inc.
FDA (openFDA food enforcement)
Reported Jul 20, 2022
MiniMed 620G Insulin Pump (O.U.S. version)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2022
epoc BGEM Test Card 25 Test Cards/box. In vitro diagnostic device for the quantitative testing of samples of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Ventana HE 600 System, automated slide preparer, for use in laboratories.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Endo Model Modular Rotational Tibia - Small (Model No #15-2814/02), Medium (Model No #15-2814/03), and Large (Model No…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2022
CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeltiq Aesthetics, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
Omnera 400T Digital Radiographic System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arcoma AB
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
SoDelicious DairyFree Wondermilk Dairy Free Frozen Dessert Salted Caramel Sundae, 3 - 4 fl oz (12 fl oz) cones per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Danone US LLC
FDA (openFDA food enforcement)
Reported Jul 13, 2022
CELLSEARCH Circulating Tumor Cell Kit (Epithelial)-IVD intended for the enumeration of circulating tumor cells (CTC) of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Menarini Silicon Biosystems
FDA (openFDA device enforcement)
Reported Jul 13, 2022
ABL800 Flex Analyzer Model Numbers 393-800 and 393-801
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Jul 13, 2022
RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one MICS injection system with Intraocular Lens:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rayner Intraocular Lenses Ltd.
FDA (openFDA device enforcement)
Reported Jul 13, 2022
Dimension LTNI -In vitro diagnostic test intended to quantitively measure cardiac troponin-I levels in human serum and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 6, 2022
System: Alphenix 4D CT in combination with CAS-930A (C arm Support) Model Number: INFX-8000C/BF, INFX-8000C/BH,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2022
DVR Anatomic, Model No. DVRAR. Distal Volar Radius Anatomical Plate System used for the fixation of fractures and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Changzhou Biomet Medical Devices Co., Ltd.
FDA (openFDA device enforcement)
Reported Jul 6, 2022
VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2022
QMS Tacrolimus Immunoassay REF 10015573 CALIBRATOR SET QMS TACROLIMUS CAL A 10015566-3 QMS TACROLIMUS CAL B 10015567-3…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
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.