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 3, 2025
Doctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21%, 4 oz./ 113.4 g per tube, Manufactured by CA Botana, San…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CA BOTANA International, Inc.
13 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 3, 2025
DermaSensor. Model/Catalog Number: 10101. Software Version: 3.0.2. Software-aided adjunctive diagnostic device for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dermasensor Inc.
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
FDA (openFDA device enforcement)
Reported Dec 3, 2025
FoundationOne CDx (F1CDx), RAL-0003 version 31.0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Foundation Medicine, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2025
IntelePACS - InteleConnect / TechPortal
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intelerad Medical Systems Incorporated
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jeni's Splendid Ice Creams LLC
FDA (openFDA food enforcement)
Reported Dec 3, 2025
CareLink Clinic, REF: MMT-7350
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Description: The Galaxy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noah Medical Corporation
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
FDA (openFDA device enforcement)
Reported Dec 3, 2025
1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel, Inc.
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Emdogain; Article Numbers: (1) 440.230V10, (2) 475.132V10;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
FDA (openFDA device enforcement)
Reported Nov 26, 2025
MONARCH Bronchoscope. Model Number: MBR-000211-B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health, Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
DxFLEX Flow Cytometer Catalog Number C78500 UDI-DI code: 15099590754013 The DxFLEX Flow Cytometer is intended for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Nov 26, 2025
Bulk and Organic Organic Moringa Powder, 44.1lbs bag
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bulk & Organic LLC
FDA (openFDA food enforcement)
Reported Nov 26, 2025
BD Alaris infusion Pump Module 8100, REF: 8100; KIT, BEZEL ASSY 8100BD, REF: 49000437; KIT ASSY ONE PIECE BEZEL 8100,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cellavision AB
FDA (openFDA device enforcement)
Reported Nov 26, 2025
Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Clot Activator Model/Catalog Number: 455071P Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
Brand Name: EZDilate Nephrostomy Balloon Catheter and Inflation Device Kit Product Name: Olympus Nephro-EZDilate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Nov 26, 2025
OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC
FDA (openFDA device enforcement)
Reported Nov 26, 2025
Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2025
TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
High riskUsing this product could cause serious injury, illness or death — stop using it now.TMJ Solutions Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new California recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.