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.
6,473 stored notices name New York, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach New York too — those are in the archive.
Reported Oct 31, 2018
LADYFINGERS GOURMET TO GO SIGNATURE SHAVED COUNTRY HAM ROLLS; ONE DOZEN PER PACKAGE (15oz - 425 grams); ALLERGEN…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ladyfingers Catering, LLC
FDA (openFDA food enforcement)
Reported Oct 31, 2018
O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027 SYSTEM PRODUCT, Model Number Bl70000027 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
APTIO INPUT/OUTPUT MODULE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Margie Cheese, Pasteurized Cow's Milk Cheese, Sprout Creek Farm Poughkeepsie, NY 12603 Plant # 36-8436
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sprout Creek Farm, Inc.
FDA (openFDA food enforcement)
Reported Oct 31, 2018
VirtuoSaph Plus Endoscopic Vessel Harvesting System, Catalog Number: VSP550EX Product Usage: The VittuoSaph¿ Plus…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Victoria Taylor's Seasonings - Blackening Rub, 6.4 oz., UPC: 666227015274, packaged in a glass jar with a lid
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Victoria Gourmet, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 24, 2018
Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 24, 2018
GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2018
La Mexicana Hot Salsa 16 oz., 24 oz., 48 oz., 64 oz., and 128 oz. Gourmet Style Hot Salsa 16 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.La Mexicana LLC
6 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 24, 2018
Mindray BeneVision Distributed Monitoring System (DMS), Part No. 115-034413-00
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula, 13Fr., REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OriGen Biomedical, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Philips HeartStart FR3 Defibrillator, Model: 861388, 861389 Product Usage: The HeartStart FR3 is used to treat…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corp.
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Quest Protein Bar Vanilla Almond Crunch Single Bar UPC# - 888849000494 12 ct. Box UPC # - 888849000500
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Quest Nutrition, LLC
FDA (openFDA food enforcement)
Reported Oct 24, 2018
Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Switzerland GmbH
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Affixus Hip Fracture Nail 125 9 mm x 180 mm, Item Number 814309180 Product Usage: Intended for the fixation of fractures
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
47 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 17, 2018
Codan Filter (Codan catalog number BC 693) used with Medrad Patient Administration Sets (PAS) and Intego PET Infusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
Colpo-Pneumo Occluder, Part CPO-6
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neomed Inc.
FDA (openFDA device enforcement)
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
Polyisoprene condomns Product Usage: The Durex Synthetic polyisoprene male condom is used for contraception and for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reckitt Benckiser LLC
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
Widex BABY hearing aid (referred to as BABY440), powered by zinc-air batteries size 10 Intended use: BABY440 is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Widex A/S
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
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)
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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.