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.
Reported Jul 11, 2018
WATERMELON CHUNKS 6/9.5Z, 9.5 oz., UPC: 81851301386; WATERMELON SPEAR 6/16Z, 16 oz., UPC: 81851301591; WATERMELON SPEAR…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Caito Foods Service, Inc.
25 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 11, 2018
ECOLAB MICROTEK Rolled Probe Cover, 2.0 cm x 20 cm (.8 in x 8 in), Ref PC0905, packaged 1 probe cover/pouch, 25…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ecolab Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
microTargeting" Drive System, Product Number MT-DS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FHC, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Jul 11, 2018
da Vinci X Surgical System, Model IS4200. Product Usage: The Intuitive Surgical Endoscopic Instrument Control System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 11, 2018
St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Medical Corp.
FDA (openFDA device enforcement)
Reported Jul 11, 2018
Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Supplement Facts Serving Size:***Vitamin B-12 (as…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Absonutrix
FDA (openFDA food enforcement)
Reported Jul 4, 2018
Space Pump IV Set, 2 Caresites, ASV, 0.2 Micron Air Eliminating Filter, Product Code 363420 The Infusomat Space Pump IV…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 4, 2018
HLD Systems 600 Series Washer/Pasteurizer, UDI (01) 0085249007009 (11) 160929 (21) 61160; Model 610HT, 115V & Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cenorin, LLC
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Amalgatome SD, COAXIAL PNEUMATIC HOSE, SCHRADER, Model X101004
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exsurco Medical
FDA (openFDA device enforcement)
Reported Jul 4, 2018
McEvoy Ranch 100% Certified Extra VirginOlive Oil; Made in California; 1 L, 33,8 FL OZ UPC 6 34832 00291
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.McEvoy
FDA (openFDA food enforcement)
Reported Jul 4, 2018
Single Chamber Temporary External Pacemaker, Model 53401
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Randox Liquid Assayed Specific Protein Control - Level 1 (SP Control 1), Cat. no. PS2682
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Safe N Simple No-Sting Skin Barrier Film, Ostomy Skin Barrier Wipe, SNS00807
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safe N Simple, LLC
FDA (openFDA device enforcement)
Reported Jul 4, 2018
ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model 10849000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Pacific Brand Charcoal Grilled Eel. Premium Quality Unagi Kabayaki UPC: 692156201099
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Supreme Foods
FDA (openFDA food enforcement)
Reported Jul 4, 2018
Diagnostic Ultrasound System, Aplio I-series. Labeled as i700, i800, i900 The power supply unit may be damaged and may…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
The BD Vacutainer Plus Plastic Citrate Blood Collection Tube is an evacuated blood collection tube that provides a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 27, 2018
CritiCore Automated Urine Output and Temperature Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
VNS Therapy Programmer, Model 3000, v1.0 System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
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.