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.
7,511 stored notices name California, reported between Jun 20, 2012 and Nov 18, 2026.
Reported Dec 18, 2019
VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943
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 Dec 18, 2019
Honey Mama s Truffle Bar (Trader Joe's) is a honey cocoa bar, refrigerated, one bar is packaged in flexible film, flow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nectar Foods Inc.
FDA (openFDA food enforcement)
Reported Dec 18, 2019
P28, Titan 3-D Wedge, Evans, Large, 10 mm, sterile, REF P03-EVN-1010-S, Type: Lagrge, Size: 10mm, (01) 00889795018182,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Ranitidine Tablets, USP 150 mg, OTC, a.) 30 count bottle (NDC 68788-7078-03), b.) 60 count bottle (NDC 68788-7078-06),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Dec 18, 2019
Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive Protein Reagent is intended for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
MRIdian Linac Radiation Therapy System Model 10000 and 20000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viewray, Inc.
FDA (openFDA device enforcement)
Reported Dec 11, 2019
XEN Gel Stent, REF 5513-001(US Model), Sterile, RX Only, (01)10888628032439 ; Other Model Numbers: 5507-001(Global…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allergan PLC
FDA (openFDA device enforcement)
Reported Dec 11, 2019
Quantam 2000 Electrosurgical Generator, Part number 909075.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 11, 2019
Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter, organic flour, organic sugar, organic eggs,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frog Hollow Farm
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Nat Cashew Flavor Type, 11.34 kg in each 4.2 gallon blue HDPE jerri-can, UPC: 20355428593
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Givaudan Flavours Corp.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Hummingbird Wholesale Organic Chia Seeds, SD120-5#, packaged in a clear plastic bag with a while label, net wt. 5 lbs.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Honey Heaven Wholesale Inc.
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Lamb Weston Grown In Idaho Crispy Hash Brown Dices, packaged in 28 ounce poly retail bags, 6 or 12 bags packaged in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lamb Weston Inc.
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Proximal Humerus Plate, 8 holes, Right, REF MDS130108R - Product Usage: The Proximal Humerus Plating System consists of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Miami Device Solutions, LLC.
FDA (openFDA device enforcement)
Reported Dec 11, 2019
TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee pain.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Theralase Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 11, 2019
Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic manual surgical instrument Item Number: 475660
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Alinity ci Level Sensor, Bulk Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxes per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Ibuprofen Oral Suspension USP, 100 mg/5mL, 4 fl.oz. 118 mL, Rx only, Preferred Pharmaceuticals, Inc., Anaheim, CA. Mfg:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Dec 4, 2019
Atellica CH 930 Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Spineart Sa
FDA (openFDA device enforcement)
Reported Dec 4, 2019
ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2019
MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 2 MASKS, Item Code 2040
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AMD Medicom Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health 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.