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 Feb 10, 2021
FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Feb 10, 2021
Nucleic acid-based in vitro diagnostic devices for the detection of 2019-novel coronavirus (2019-nCoV) and/or diagnosis…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biomeme, Inc.
FDA (openFDA device enforcement)
Reported Feb 10, 2021
Neuroreader Medical Image Processing Software - Product Usage: intended to automate the current manual process of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainreader ApS
FDA (openFDA device enforcement)
Reported Feb 10, 2021
Philips EPIQ Diagnostic Ultrasound System; Model Numbers: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 7G, EPIQ 7C, EPIQ CVx &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2021
SARS-CoV-2 Antigen Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
FDA (openFDA device enforcement)
Reported Feb 10, 2021
Optilite Freelite Mx Kappa Free Kit REF LK016.M.OPT.A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Feb 10, 2021
Harmony Referral System (aka Harmony RS)/ Medical Device Data System - Product Usage: intended to be used by trained…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Topcon Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 3, 2021
BD Stimex Insulated Needle 22G x 2.13in ( 50 units/cs.) Indicated for administration of medications to affect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 3, 2021
B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Braxton Medical Corporation
FDA (openFDA device enforcement)
Reported Feb 3, 2021
DRW-0739-01:Gen 2 Anterior Chairside Splint LRUL (lower right-upper left); accessories to the parent system, the Neocis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neocis, Inc.
FDA (openFDA device enforcement)
Reported Feb 3, 2021
PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No. 01454 RoHS Compliant; PSG-100 Head Box; UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nihon Kohden America Inc.
FDA (openFDA device enforcement)
Reported Feb 3, 2021
SERF Novae Dual Mobility Cup Insert 51/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OMNIlife science Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 3, 2021
Tegral Satin EC CL Vegan Cake packaged in 50lbs bags
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Puratos Corporation
FDA (openFDA food enforcement)
Reported Feb 3, 2021
Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respironics California, LLC
32 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 3, 2021
Samyang Buldak Extremely Spicy Hot Chicken Flavor Sauce Hot Chili Sauce Net Wt. 200 g (7.05 oz) Product of Korea UPC: 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Samyang Foods Co. Ltd.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 3, 2021
Weis Quality Cookies and Cream Ice Cream (48oz). Packaged in a squround paper container with a UPC of 041497-01253.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Weis Markets, Inc., Ice Cream Division
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 27, 2021
ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG REF C58964 - Product Usage: use on the Access Family of Immunoassay Systems…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jan 27, 2021
JTM FOOD GROUP brand READY TO EAT WHITE CHEDDAR MACARONI & CHEESE in 5 lb. plastic bags, 6 bags per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JTM Provisions Co. Inc.
FDA (openFDA food enforcement)
Reported Jan 27, 2021
Frozen Tuna Ground Meat - Khee Trading Brand Product of Vietnam 22 Lb. Cartons (2 x 11 lb.)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Khee Trading, Inc.
FDA (openFDA food enforcement)
Reported Jan 27, 2021
REF 27219-1 X1, Medtronic, Delta Valve, Neonatal, Performance Level 1.0, CE 0344, Sterile EO - Product Usage: Neonatal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 27, 2021
Penumbra JET 7 Reperfusion Catheter REF 5MAXJET7 The Penumbra JET 7 Reperfusion Catheter with Xtra Flex technology (JET…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Penumbra Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 27, 2021
FITNESS LABS***Organic***Coconut Oil***Extra Virgin***16 fl. oz. (473 mL)***Carefully Designed and Distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Piping Rock Health Products
FDA (openFDA food enforcement)
Reported Jan 27, 2021
OsteoVation, Inject Bone Filler Kits, 5cc (part number 390-2005, manufacturing lot number 1129957) - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skeletal Kinetics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 27, 2021
Neurosign 100, Product Number 9883-01. Intraoperative Nerve Monitor - Product Usage: indicated for use in stimulating…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Magstim Company Limited
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.