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 Dec 16, 2020
MAC VU360, Electrocardiograph
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Dec 16, 2020
Golden Boy brand Custard muffin Original; 7.76 ounce, rigid clear plastic packages
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hong Thai Foods Corp.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 16, 2020
On the Go Sweet & Salty Trail Mix
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kanan Enterprises Inc.
FDA (openFDA food enforcement)
Reported Dec 16, 2020
Shimadzu Mobile X-Ray System, MobileDaRt Evolution (MX8 Version), with adjustable handle option, Made in Japan -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 16, 2020
Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Ltd.
FDA (openFDA device enforcement)
Reported Dec 16, 2020
PROKERA, non-sterile - Product Usage: Biologic corneal bandage.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TissueTech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 16, 2020
1. Fresh Attitude Baby Spinach, 11 oz. 2. Fresh Attitude Baby Spinach, 5 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Veg Pro International Inc.
FDA (openFDA food enforcement)
Reported Dec 16, 2020
ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn, Inc/mortara
FDA (openFDA device enforcement)
Reported Dec 9, 2020
The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in vitro diagnostic test that is based on widely used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomeme, Inc.
FDA (openFDA device enforcement)
Reported Dec 9, 2020
6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva, Order No. 73039 - Product Usage: The kit is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chromsystems Instruments & Chemicals GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 9, 2020
REF MC330209 6' (15 cm) Appx 0.09 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 0.2 Micron Filter, 1.2 Micron…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 9, 2020
B. Braun Introcan Safety IV Catheters, Product codes REF 4252500-01 4252519-01 4252535-01 4252560-01 4252586-01…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Janus Trade Group
FDA (openFDA device enforcement)
Reported Dec 9, 2020
Chlorhexidine Gluconate Oral Rinse USP, 0.12%, Alcohol Free, packaged in 15 mL unit does cups (barcode 7016602715),…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lohxa LLC
FDA (openFDA drug enforcement)
Reported Dec 9, 2020
Quantum Health branded Elderberry liquid herbal extract dietary supplement is packaged in 2oz glass bottle, 12…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Quantum Inc.
FDA (openFDA food enforcement)
Reported Dec 9, 2020
BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2020
Continental Glatt Kosher Meats Corp. Recalls Ready-To-Eat Meat and Poultry Products Produced Without Benefit of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Continental Glatt Kosher Meats Corp.
USDA FSIS
Reported Dec 2, 2020
AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Advanced Bionics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloplast Manufacturing US, LLC
FDA (openFDA device enforcement)
Reported Dec 2, 2020
EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom Manufacturing, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the Ion Fully…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
ViewRay MRIdian System: Model No. 10000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viewray, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Art Of Tea - Feel Better tea; Produced and Distributed by: Art of Tea LLC, Monterey Park, CA Directions: 1 Tbsp of tea…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Art Of Tea
FDA (openFDA food enforcement)
Reported Nov 25, 2020
Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product 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.