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 Sep 22, 2021
Arjo Disposable Repositioning Sling, Model AHD001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Dominican Republic SA
FDA (openFDA device enforcement)
Reported Sep 22, 2021
Potassium Hydroxide 10% (KOH 10%), Cat. No. 300145 Potassium Hydroxide 10% (KOH 10%) is intended for use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gibson Bioscience
FDA (openFDA device enforcement)
Reported Sep 22, 2021
Vita Aid Keto-Elemental Nutrition (Chocolate), VA-958. The product is a powder, packaged in an aluminum bag , with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Naturo Aid Pharmaceutical Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 15, 2021
Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each and 2.5kg sample…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ingredion
FDA (openFDA food enforcement)
Reported Sep 15, 2021
Pipeline Flex Embolization Device
High riskUsing this product could cause serious injury, illness or death — stop using it now.Micro Therapeutics Inc.,
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 15, 2021
Nihon Kohden NKV-550 Ventilator, REF: NKV-550-U, CE 0344, UDI: (01) 00843685100012 The Nihon Kohden NKV-550 Series…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nihon Kohden Orangemed, Inc.
FDA (openFDA device enforcement)
Reported Sep 8, 2021
TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 8, 2021
Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hostess Brands, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 8, 2021
12 PC Shrimp Tempura Kabuki Roll [BR] UPC: 81244803670 Products were sold from Genji Sushi counters inside Whole Foods…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mai Cuisine
24 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 8, 2021
MY01 Continuous Compartmental Pressure Monitor, Reference Number MY01-0001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.My01, Inc.
FDA (openFDA device enforcement)
Reported Sep 8, 2021
Gyrus Acmi PKS Omni 5mm/33cm-intended for the electrosurgical coagulation, mechanical grasping, and dissection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Sep 8, 2021
Artis Models with SW version VD12 listed below: Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee MP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 8, 2021
EL-Anti-SARS-CoV-2 IgM Kit, Catalog #104-129, IVD. Submitted as EUA202129
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thera Test Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 8, 2021
CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of SARS-CoV-2 Antigen Qualitative detection of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Versea Diagnostics LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 8, 2021
Cahill Cheddar with Porter PLU 93579 packaged in clear plastic
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 8, 2021
CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeltiq Aesthetics, Inc.
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Normand Remisol Advance Data Manager, REF: C69412, C69413, C44703, and C57017 is a software device that interfaces…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 1, 2021
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMimetic Therapeutics, LLC
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardinal Health
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 1, 2021
AltiVate Anatomic Shoulder System for the following Part Numbers: 1. Part # 520-08-00, Rev. C., 2. Part # 520-10-000,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Sep 1, 2021
NES Reprocessed Visions PV .035 IVUS Catheter, Sterile. For use in the evaluation of vascular morphology in blood…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Northeast Scientific Inc.
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Ingenia 1.5T Evoluton- Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 1, 2021
AQUABEAM Handpiece, REF: HP2000, a sterile single-use component of the AQUABEAM Robotic System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Procept Biorobotics Corporation
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 Fr, Guidewire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W. L. Gore & Associates 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.