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.
7,493 stored notices name California, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported Oct 28, 2026Updated Nov 2, 2026
Voila! juice 100% SQUEEZED ORANGE VOILA! OAKLAND, CA 94601 16 OZ: UPC 701725001074 32 OZ: UPC 701725001081 64 OZ: UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Voila Juice Company
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Wild West Seeds Broccoli Seeds Green Sprouting Calabrese lot #4105. Net Wt. 50lb. Wild West Seeds Broccoli Waltham29…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wild West Seed Inc.
FDA (openFDA food enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Nov 2, 2026
Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel plus Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture, 1X18" TF-5, Product Code: N271H
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, LLC
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009802028. in vitro diagnostic (OUS only)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Instrumentation Laboratory
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
JenaValve Trilogy Delivery Catheter, Size 27MM REF: TRILOGY-DC-L
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jenavalve Technology Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Magellan Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Standard for use with the SCOUT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, REF: OPRO-101; MAS Omni IMMUNETM PRO Liquid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AVID Medical, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Biospectra Tris/Tromethamine, USP, GMP, API Grade, Manufactured at 100 Majestic Way, Bangor, PA 18013, NDC 64173-101-25
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioSpectra, Inc.
FDA (openFDA drug enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.G L Mezzetta Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intellijoint Surgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
TufTex¿ Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LeMaitre Vascular, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Generic Name: Kit, Urine, Clean Catch Trade Name: Kit: Urinary Clean Catch 20/cs Model/Catalog Number: 76769 Lot…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medical Action Industries, Inc. 306
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nihon Kohden America LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Onkos Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pepsico Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
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.