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.
In the agency's Nov 11, 2026 enforcement report
Generic Name: Edwards Commander M Delivery System Generic Name: Edwards Commander M Delivery System Model/Catalog…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (weekly enforcement report)
In the agency's Nov 11, 2026 enforcement report
Nextseq 550Dx Instrument REF: 20005715, FOR IN VITRO DIAGNOSTIC USE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
2 more products in this recall
FDA (weekly enforcement report)
In the agency's Nov 11, 2026 enforcement report
Tandem Mobi Insulin Pump, Models: 1004004, 1010750, 1012676, 1012719, 1013655, 1013656, 1013501, 1013700, 1014081,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tandem Diabetes Care, Inc.
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
EMAG system Model/Catalog Number: 418591/418591U Product Description: Nucleic acid sample preparation instrument IVD,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
Nalu TD2 Therapy Disc with firmware, REF: 34014-001, and TD2 Patient Kit, REF: 74011, part of the Nalu Neurostimulation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
ALPHENIX INTERVENTIONAL ANGIOGRAPHY SYSTEM REF: INFX-8000C
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
EDEN BROTHERS Broccoli Seeds - Calabrese. Sold in packets, Net Wt. 1oz pouches, UPC SVBRO111 -qb2 & 1 Pound pouches UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eden Brothers
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
ETHILON Nylon Suture, Product Code 697G
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, LLC
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
OmniaSecure Model 3930M, LEAD 3930M74 74 CM DF4 MR 3930M74 LEAD 3930M79 79 CM DF4 MR 3930M79 The Medtronic OmniaSecure"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic, Inc.
1 more product in this recall
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
Blue Bottle Coffee 4oz Sweet Blossom Simple Syrup in a glass boston round bottle with metal and plastisol cap. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pink House Alchemy, LLC
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
Precision Pointer Electromagnetic (8000-050-001)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Leibinger GmbH & Co. KG
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
Sunny Sky Non-Dairy French Vanilla Creamer, 96oz , bag in box, 3 per case, refrigerate after opening.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sunny Sky Products, LLC
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
Orthoscan VERSA Accessory Cart, REF: 1000-0021 and Versa Mini C-Arm System, REF: 1000-0020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziehm-Orthoscan Inc.
FDA (weekly enforcement report)
FoodReported Oct 30, 2026Updated Nov 3, 2026
Once Upon A Farm Recalls All Lots and Varieties of Tractor Wheels Organic Toddler Soft-Baked Bars Due to Potential Choking Hazard
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Once Upon A Farm
FDA (recalls & safety alerts)
Reported Oct 28, 2026Updated Nov 2, 2026
PNE Lead Implant Kit REF: 1701
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Axonics, Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
B Braun SAFSITE Injection Site, RV1000NC SAFSITE VALVE W/O EXTRA CAP. Catalog Number: 415068.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Raw In-Shell Peanuts; packed in a clear plastic 1lb, 5lb, 50lb unit sizes. Raw Spanish Peanuts; sold by weight (bulk)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.El Ruisenor De Mexico, Inc.
12 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
GEARHARTS FINE CHOCOLATES Net Wt. 4oz UPC 8 98111 00205 7; Net Wt. 8oz UPC 8 98111 00206; Gearharts Fine Chocolates…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gearharts Fine Chocolates, Inc.
FDA (openFDA food enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Ion Torrent Genexus Dx with software, Catalog: A40003539, which supports the Ion Torrent Genexus Dx Integrated Sequencer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Holdings Pte Ltd.
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
MEDLINE DRAPE C-SEC FEN CLEAR SCRN WIRE, Medline Product Number/SKU DYNJP6106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Medtronic NDI Passive Spheres REF: 8801075, Sterile EO, 5/Tray 12 Pk., Rxonly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Philips Lumify Diagnostic Ultrasound System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Ultrasound, LLC
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Sempio Yellow Peach; Product of Korea; NET WT. 14.10 oz. UPC: 8801005320825
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sempio Food Services, Inc.
FDA (openFDA food enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Xact mole marker for mammography Model/Catalog Number: M15RM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Solstice Corporation
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.