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.
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)
Reported Aug 25, 2021
Cell Marque Antibodies, PSA (ER-PR8) Mouse Monoclonal Antibody, REF: 324M-15, 324M-16
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cell Marque Corporation
FDA (openFDA device enforcement)
Reported Aug 25, 2021
Chicken of the Sea Genova Meal Kit; Kits include dry whole wheat pasta, dried basil and parsley, 2 cans of Genova Tuna,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chicken of the Sea; Thai Union
FDA (openFDA food enforcement)
Reported Aug 25, 2021
Moonwalk 70% dark chocolate bar. It is packaged in white shiny paper with blue print. Net Weight: 1.2 oz / 35gr. No…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cocanu LLC
FDA (openFDA food enforcement)
Reported Aug 25, 2021
Cytocell LPH019-A E2A (TCF3) Breakapart Probe- In Vitro Diagnostic Analyte specific reagents (ASR's)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cytocell Ltd.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
NEO-KATH Epidural Catheter Set, REF 200-2430, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epimed International
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2021
CIRCUL8 LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF: 08-0020, Rx Prescription Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho8, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2021
EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
The Aequalis Pyrocarbon Humeral Heads. Shoulder implant component. Sold OUS only: a) Catalog # DWH039 - Diameter 39 mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier S.A.S.
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.