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 48,122 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported May 16, 2018
Connecting Tube - Female to Male Luer Lock, HPCT8.8-60-M-FM Product Usage: The connecting tube is intended to be a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
BEQ-T 9410 Lurie Chldns Small 1/4, Custom Tubing Kit, Catalog No. 709000430
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Datascope Corporation
27 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostic Hybrids, Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
Fabius MRI, anesthesia machine, catalog no. 8607300 Product Usage: The products are inhalation anesthesia machines for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
Eden's Ethnos Bulk Kratom 25 powder kilogram bag Also called K. Bali Supreme, K Maeng Da Supreme, K Green Vein, Green…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eden's Ethnos, LLC
FDA (openFDA food enforcement)
Reported May 16, 2018
Hemodynamic monitoring system (HMS), comprised of a Patient Interface Module (Part Number 58401-000 and a User…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported May 16, 2018
EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MHC Medical Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz (84g); UPC: 853787005368
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Munk Pack Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 16, 2018
NvisionVLE¿ Low-Profile Optical Probe; Catalog Numbers: 95501-LP and 95501-LP-5; UDI Information:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ninepoint Medical Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
Sterile Aquasonic 100 Ultrasound Transmission Gel, 20 grams, Model Number 01-01-4, 400 packets/case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Parker Laboratories, Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
NeoBase Succinylacetone Assay Solution, Product Number: 3042-0020; Affected UDI Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Life and Analytical Sciences, Wallac, OY
FDA (openFDA device enforcement)
Reported May 16, 2018
ACUSON SC2000 Ultrasound System. The firm name on the label is Siemens Medical Solutions USA, Inc., Buffalo Grove, IL.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
STONEWALL KITCHEN Basil Pesto Aioli Net Weight Net 10.25 oz. UPC: 7 11381 03060 8. Product is incorrectly labeled as…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stonewall Kitchen, LLC
FDA (openFDA food enforcement)
Reported May 16, 2018
Sugarfina Platinum Bling Ring; Product SKU No. R-1790 UPC: 840278116139 Net W. 21g ().7 oz.) Sculpted from dark…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sugarfina, LLC
FDA (openFDA food enforcement)
Reported May 16, 2018
Jasper Vektor, Class II Correction Appliance, Part No. 610-500 used for correcting class 2 malocclusions by applying…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TP Orthodontics, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
Raw Form Organics Maeng Da Kratom Emerald Green; 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Triangle Pharmanaturals LLC
25 more products in this recall
FDA (openFDA food enforcement)
Reported May 16, 2018
PICC Kit, Product Code: AMS-7063-1 Convenience kit for the insertion of PICCs into the vascular system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vygon U.S.A.
7 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
Lactosorb RapidFlap, bone plate, Model No. 915-0020 The RapidFlap LS Cranial Fixation System is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 9, 2018
BD MAX DNA MMK (SPC) For Laboratory Use, catalog no. 442829
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 9, 2018
StoneBreaker Pneumatic Lithotripter, Catalog number: SBL-KIT1; GPN: G52604 UDI:(01)00827002526044
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 9, 2018
Ignite High Endurance Pre-Workout Supplement with Caffeine, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01540 2.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Independent Nutrition, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported May 9, 2018
Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule Endoscope System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IntroMedic Co., Ltd.
FDA (openFDA device enforcement)
Reported May 9, 2018
Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America 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.