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 Oct 17, 2018
OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, REF ZBH-PSNCREF311-L.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosensor, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 17, 2018
Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product; Net Wt. 70 G/Cookie; Contains: Flour, eggs, Baking Soda,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sarap Asian Fusion
3 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 17, 2018
Reprocessed Agilis Steerable Introducer: indicated for introducing various cardiovascular catheters into the heart. (a)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sterilmed, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
FDA (openFDA device enforcement)
Reported Oct 11, 2018
Valley Fine Foods Retira Productos De Carne De Res Y Aves Debido A Una Posible Adulteracin
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Oct 10, 2018
Trader Darwin s Chewable Peppermint Flavored Melatonin Dietary Supplement Number of units per package: 100 tablets…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Church & Dwight Co.
FDA (openFDA food enforcement)
Reported Oct 10, 2018
Laparoscopy Instruments Instructions For Use (IFU) for the following: 1)Monopolar electrode, 2) Insert, handle and/or…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dannoritzer Medizintechnik GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Oct 10, 2018
ENDOLOGIX AFX Endovascular AAA System, Stent Graft System, Rx Only, Sterile EO, REF: BA22-120/I20-40, BA22-100/I20-40,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Endologix
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2018
ICU Medical 14" (36 cm) Appx 3.6 ml, Bifuse Transfer Set w/Rotating Luer, REF: 14237-28 The Intravascular…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported Oct 10, 2018
Formed Hash Brown Patties, packaged in cardboard trays covered with plastic film, frozen products. The following brands…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lamb Weston Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 10, 2018
Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2 lbs. (907.18g)**Nutrition facts***Ingredients:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Neighbors LLC
FDA (openFDA food enforcement)
Reported Oct 10, 2018
smiths medical portex First Breath Adult Nasal Cannula, REF 001283, Non-flared Tips, 213 cm (7 ft.) Tubing,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Smiths Medical ASD Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2018
TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy Delivery System version 2.0 and 2.5 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2018
EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wismettac Asian Foods (USA) dba Nishimoto Trading Co. Ltd.
FDA (openFDA food enforcement)
Reported Oct 3, 2018
DX-D 600 Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imaging system used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Agfa N.V.
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Bausch + Lomb Stellaris Elite 20 GA Vit Cutter, Model BL5626, 7500 cpm, packaged in sterile pouches, 6/shipper.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2018
ESSENTIO Pacemaker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2018
FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Confidence Inc./Confidence U.S.A. Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 3, 2018
Retractor System Elastic Stays (Part 3314-lG; 3316-lG; 3550-lG) Product Usage: The Retractor System Elastic Stays (Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the following product name sold under: Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Visualase Thermal Therapy System, Software: Visualase Software versions 3.1.1 - 3.2, Product #: 9735542
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Medtronic DxTerity(TM) TRA 5F, Diagnostic Catheter, REF U5TRAN35
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medtronic Vascular
FDA (openFDA device enforcement)
Reported Oct 3, 2018
INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
26 more products in this recall
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.