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.
Reported Sep 23, 2026
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, Inc.
1 more product in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bd Switzerland Sarl
FDA (weekly enforcement report)
Reported Sep 23, 2026
Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Happiest Baby, Inc.
1 more product in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
Plum administration sets
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
7 more products in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
Intercon Foaming Pear Hand Soap With Aloe, 28.7 fl. oz., Manufactured for: Intercon Chemical Company 1100 Central…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intercon Chemical Co.
5 more products in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
Philips Patient Information Center iX REF:866389
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
1 more product in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
GM Helix Implant, REF: 109.984;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
FDA (weekly enforcement report)
Reported Sep 16, 2026
Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
5 more products in this recall
FDA (weekly enforcement report)
Reported Sep 16, 2026
HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (weekly enforcement report)
Reported Sep 16, 2026
Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Sprout Holdings, Inc.
FDA (weekly enforcement report)
Reported Sep 16, 2026
Red Blood Cells, Leukocytes Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stanford Blood Center LLC
1 more product in this recall
FDA (weekly enforcement report)
Reported Sep 16, 2026
AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
FDA (weekly enforcement report)
Reported Sep 9, 2026Updated Sep 14, 2026
Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AVID Medical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
19 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
STA Staclot Protein S, Model/Catalog Number: 00746-Reagent Lot number 273074; qualitative and quantitative factor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
OLA-OLA Pounded Yam (Iyan) IYANINSTANT, NET WT. 2 lbs., 4 lbs., 5 lbs., 10 lbs, packed in flexible plastic bags.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fayus Inc.
FDA (openFDA food enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 16, 2026
Schwarzkopf Professional Osis Grip Mousse; 6.76 fl. Oz/200ml; aluminum can
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Henkel Consumer Goods Inc.
FDA (weekly enforcement report)
Reported Sep 9, 2026Updated Sep 14, 2026
HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 16, 2026
Food to Live brand Organic Supergreens mix (kale, moringa leaf, wheat grass, & spirulina), 8 oz, 1 lb, 1.5 lb, 3 lb, 6…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lexunder Inc.
FDA (weekly enforcement report)
Reported Sep 6, 2026Updated Sep 17, 2026
Prime Line Distributors, Inc. and Ferrarini USA, Inc. Recall Imported Ready-To-Eat Pork Guanciale Products Due to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Sep 2, 2026Updated Sep 13, 2026
Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Byron White Formulas, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2026Updated Sep 7, 2026
Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiography/fluoroscopy system used in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, 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.