Recalls distributed in New York
These notices name New York 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.
6,374 stored notices name New York, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach New York too — those are in the archive.
Reported Oct 28, 2020
BD Nexiva Closed IV Catheter System Dual Port (20 GA 1.75 IN) Catalog (Ref) No. 383538 BD Nexiva closed IV catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) X 105 cm Expiration Date June 8th 2021 - July 22nd 2021…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Oct 28, 2020
System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
High Quality Organics Organic Parsley, Medium, Organic Parsley Fines 50 lbs. 25 lbs. 20 lbs. 0.25 lbs.
High riskUsing this product could cause serious injury, illness or death — stop using it now.High Quality Organics
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 28, 2020
NanoClave Connector; 1 unit per pouch, 100 multivac pouches per case;UDI (01)10887709051017(17)241201(30)100(10)4549051;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
98 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Invivo Corporation
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to be used with an Olympus TV camera system, light…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
40 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Langston Dual Lumen Catheter
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Shirakiku brand Black Fungus (Kikurage); 5 lb. bag, 6 x 5 lb. bags per case Item # 60403; UPC 0 74410 60403 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wismettac Asian Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 21, 2020
Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health" PROTEXIS" Latex Micro Surgical Gloves - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Oct 21, 2020
Servo-i Ventilator, Part No. 6487800, UDI Code 07325710000823 - Product Usage: intended for general and critical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Group Logistics America, LLC
FDA (openFDA device enforcement)
Reported Oct 21, 2020
SwiftHook sold as the following: a. Individually as SwiftHook b. Included with Vega505EE mobile lifts Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Handicare AB
FDA (openFDA device enforcement)
Reported Oct 21, 2020
Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizuho OSI
FDA (openFDA device enforcement)
Reported Oct 21, 2020
ADVIA Chemistry Systems-Fructosamine (FRUC)-For in vitro diagnostic use in the quantitative measurement of glycated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2020
SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product Usage: is a high quality, self-contained…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skytron, Div. The KMW Group, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2020
MICROFLEX Diamond Grip Examination Gloves, MF-300 - Product Usage: A patient examination glove is a disposable device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Healthcare Products LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2020
BellaTek Encode Defin3DPMSERitive Abutments-3D Printed Model Reference Numbers: 3DPMSER, 3DPMSERQ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 14, 2020
DJO EMPOWR Tibial Knee Punch Handle Part No. 801-05-040 and 801-05-018 contained in Instrument Tray for EMPOWR Porous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Oct 14, 2020
SKIPPY Super Chunk Peanut Butter 16.3oz UPC: 00037600110723 packaged in non-flexible plastic container
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hormel Foods Corporation
FDA (openFDA food enforcement)
Reported Oct 14, 2020
"Nettle Meadow Artisan Cheese *** Fig Honey Fromage Frais*** Contains pasteurized goat and cows milk*** 5 oz.***"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LuMaZu, LLC dba Nettle Meadow
4 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 14, 2020
DABRA RA-308 Excimer Laser, SN: ******* - Product Usage: The device is intended for use in ablating a channel in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ra Medical Systems, 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.