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 Dec 31, 2025
LifeShield Drug Library Management (DLM); LifeShield Infusion Safety Software Suite v2.2 List Number 17003-02
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2025
da Vinci 5, Surgeon Console Column Motor Connector; ASSY,DV5 CONSOLE,SSC,IS5000; Part Number: 380730-40
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Dec 31, 2025
Product: Zimi Puff Pastry French Style (frozen) Package Size and quantity per case: 700 g paper carton - 12/case UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karabetian Import and Distribution, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 31, 2025
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
16 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 27, 2025
Mountain West Food Group, LLC Recalls Ground Beef Products Due To Possible E. Coli O26 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mountain West Food Group LLC
USDA FSIS
Reported Dec 24, 2025
Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2025
1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Copan Italia
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Intelerad InteleShare software, with ProViewer component
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DICOM Grid, Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant Model/Catalog Numbers: 600-601 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dsaart LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Software for the controlled administration of fluids to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresenius Kabi USA, LLC
FDA (openFDA device enforcement)
Reported Dec 24, 2025
HemosIL SynthAFax. Partial Thromboplastin Time Tests.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Instrumentation Laboratory
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 2…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lexunder Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 24, 2025
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2025
InPen App, Model/CFN Number: MMT-8061 (Android Users)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Myosa for Kids KS1 REF MyOSAKS1_Sb/Sp/Mb/Mp/Lb/Lc KS2 REF MyOSAKS2_Sb/Sc/Mb/Mc/Mp/Lb/Lc Myosa for Kids is a mouthguard…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Myofunctional Research Company USA
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Dec 24, 2025
BIOSURE HA SCREW, 6MM x 20 MM. Threaded metallic bone fixation fastener.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2025
SENNA LEAVES F/C OG Item No: SEN15001 Net Wt: 44.75 Lbs Distributed By Whole Herb Company 19800 8th Street East,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Whole Herb Company, Inc.
FDA (openFDA food enforcement)
Reported Dec 17, 2025
Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2025
Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 17, 2025
ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction of respiratory gases between the breathing…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 17, 2025
Doughy brand Chocolate Chip Cookie Dough; 12 oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hudson River Foods Corp.
FDA (openFDA food enforcement)
Reported Dec 17, 2025
3 B Cookware 4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.India's Fine Foods, Inc.
2 more products in this recall
FDA (openFDA food 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.