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.
6,466 stored notices name New York, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach New York too — those are in the archive.
Reported Mar 3, 2021
ENROUTE Transcarotid Stent System REF SR-XXYY-CS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Silk Road Medical Inc.
FDA (openFDA device enforcement)
Reported Mar 3, 2021
Tube Tracheostomy and Tube Cuff, Bivona¿ Cuffless Neonatal/Pediatric FlexTend" Tracheostomy Tube (model 60PFS45, lots…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Mar 3, 2021
OT1000 Series Orthopedic Surgical Tables
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Feb 24, 2021
13C-Spirulina Gastric Emptying Breath Test (GEBT) - Product Usage: intended for use in the measurement of the rate of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cairn Diagnostics
FDA (openFDA device enforcement)
Reported Feb 24, 2021
IOLMaster 700
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
FDA (openFDA device enforcement)
Reported Feb 24, 2021
Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Confirm Biosciences Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 24, 2021
System, X-Ray, Tomography, Computed: Revolution Apex, Revolution CT with Apex Edition
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 24, 2021
Getinge CM320 Series Washer Disinfector - Product Usage: A multi chamber washer disinfector intended for washing,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Group Logistics America, LLC
FDA (openFDA device enforcement)
Reported Feb 22, 2021Updated Oct 23, 2026
GLG Trading Inc., Recalls Beef Tallow Products Imported Without the Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.GLG Trading Inc.,
USDA FSIS
Reported Feb 17, 2021
Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18S, 1/18 GA Flexcore Biopsy Needle, 1/7F…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 17, 2021
Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arjohuntleigh Magog, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2021
Cook Medical Kwart Retro-Inject Ureteral Stent Set 7.0Fr. 22-32cm -Used for retrograde injection during Extracorporeal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2021
Universal Femoral Sleeves - Product Usage: used primarily in revision surgeries with the S-ROM Noiles, LPS, SIGMA, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2021
Infinity Acute Care System (IACS) Monitoring Solution: The IACS is intended for multi-parameter, physiologic patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draegar Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2021
"LAVVA Blueberry Dairy Free Pili Nut Yogurt. NO SUGAR ADDED. NET WT 5.3OZ (150g) ***KEEP REFRIGERATED***DISTRIBUTED BY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Evr Foods Inc.
FDA (openFDA food enforcement)
Reported Feb 17, 2021
GE Healthcare Precision 600FP, Classical R&F (radiographic and fluoroscopic) System - Product Usage: Intended for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Feb 17, 2021
60 IN (152cm) APPX 1.5 ml, PUR YELLOW SMALLBORE SET, FILTER REF B2209 - Product Usage: The intravascular administration…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 17, 2021
Maine Grains Inc. brand Organic Yellow Peas sold between 10/17/2019 and 11/1/2020; product was packaged in 25lb bulk…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maine Grains, Inc.
FDA (openFDA food enforcement)
Reported Feb 17, 2021
PRYTIME MEDICAL REBOA Catheter Introducer Kit, REF: KT1835C, Contents: Needle, 18 GA x 7 CM ECHOGENIC, STERILE, 1 EA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prytime Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Feb 10, 2021
Amy's Soups made with organic Lentils - Golden Lentil - Indian Dal. Net Wt. 14.4 oz (408g) Ready to serve - do not add…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amys Kitchen Inc.
FDA (openFDA food enforcement)
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)
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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.