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 Sep 23, 2020
The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) - Product Usage: Instructions for Use - Centrifugal Pump…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Sep 23, 2020
NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and communication system software that retrieves,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novarad Corporation
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Wegmans Vanilla Trifle; 9oz; UPC 7789080600
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wegmans Food Markets, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 16, 2020
Back to Nature, Organic Rosemary and Olive Oil Stoneground Wheat Cracker, 6 oz. foil bag inside paper carton, 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B&G Foods North America, Inc.
FDA (openFDA food enforcement)
Reported Sep 16, 2020
BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009, Length 3.8; 2025-03-18 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hager & Meisinger GmbH
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hellofresh US
FDA (openFDA food enforcement)
Reported Sep 16, 2020
Ion Catheter Reprocessing Cover, IF1000 (Part Number:490114-02) UDI:00886874116845.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Merge PACS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Blanxart 82% Congo Organic Chocolate Bar. Paper packaging with internal foil wrapper. Net weight per bar: 4.4 oz. UPC 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Power Selles Imports dba Culinary Collective
FDA (openFDA food enforcement)
Reported Sep 16, 2020
QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
FDA (openFDA device enforcement)
Reported Sep 16, 2020
SOUTHERN GROVE; MIXED NUTS; LESS THAN 50% PEANUTS; PEANUTS, ALMONDS, CASHEWS, HAZELNUTS, & PECANS; with Sea Salt; NET…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Superior Nut Company, Inc.
FDA (openFDA food enforcement)
Reported Sep 9, 2020
BD Alaris System. The EtCO2 module is a capnograph indicated for continuous, noninvasive monitoring of end tidal carbon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Parvovirus B19 IgG EIA kit Part No. V519IGUS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diasorin Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Newman's Own Organics, Newman's Special Decaf Medium Roast, Ground Coffee, 10 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keurig Dr Pepper, Inc.
FDA (openFDA food enforcement)
Reported Sep 9, 2020
Symbia S-Series and Symbia T-Series - Product Usage: Intended use of the device SPECT: To detect or image the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stimwave Technologies Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2020
SUNDIAL (4 oz.) ETHIOPIAN TENADAM HERB; "***Strengthens the Vein & Capillaries***lowers high Blood pressure, regulate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sundial Herbal Products
67 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 9, 2020
Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster (israel), Ltd.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Flexible Intubation Fiberscope, Part: 11301AA1, with Instruction Manual: Z18441US - Product Usage: are intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Klarity Vacuum Bags, Item Nos. R7504-30C, R7504-35BC,R7504-35C, R7644-32.5BC, RC7221-25BC, RC7504-17.5C - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Klarity Medical Products LLC
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.