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 Nov 8, 2023
Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quest Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 1, 2023
TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: TDC0005Z and TDC0005
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acclarent, Inc.
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Betty Lou's Inc.
FDA (openFDA food enforcement)
Reported Nov 1, 2023
Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardinal Health 200, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 1, 2023
SOZO Bilateral Arm L-Dex Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Impedimed Limited
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Organic Protein & 50 Superfoods Protein Powder with Probiotic - Chocolate flavor
High riskUsing this product could cause serious injury, illness or death — stop using it now.Orgain
FDA (openFDA food enforcement)
Reported Nov 1, 2023
Astral 100 and Astral 150 ventilators
High riskUsing this product could cause serious injury, illness or death — stop using it now.ResMed Ltd.
FDA (openFDA device enforcement)
Reported Nov 1, 2023
SynCardia 50cc TAH-t, Clinical, REF 570500, Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SynCardia Systems LLC
FDA (openFDA device enforcement)
Reported Nov 1, 2023
One Step Pregnancy Test REF 100-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Universal Meditech Inc.
26 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 25, 2023
Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
FDA (openFDA device enforcement)
Reported Oct 18, 2023
GAMMEX NON-LATEX PI GREEN Surgical gloves, REF: 20685255 through 20685290
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Healthcare Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 18, 2023
Procedure packs: (1) Presource Pain Tray, Catalog SBAHFPTAS2, Advanced Surgery Center SAR, Sterile. (2) Presource Block…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 18, 2023
BD Pyxis CII Safe ES, REF: 1116-00; and BD Pyxis : CII Safe ES Desktop PC, Wired SCNR, REF: 107-254-01; CII Safe ES…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Oct 18, 2023
REVERSE PROSTHESIS SHOULDER SYSTEM, SCREW, LOCKING BONE, RSP, 5mmX30mm long, REF: 506-03-130
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 18, 2023
Evivo with MCT Oil Infant Probiotic Activated B. infantis EVC001 (ActiBif) For Enteral or Oral Administration…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Infinant Health, LLC
FDA (openFDA food enforcement)
Reported Oct 18, 2023
Maisie Jane's Smooth almond butter, 12 oz glass jar, 6 units per case, shelf stable
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maisie Jane's California Sunshine Products Inc.
FDA (openFDA food enforcement)
Reported Oct 18, 2023
CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RoyalVibe Health Ltd.
FDA (openFDA device enforcement)
Reported Oct 18, 2023
LittleOak Natural Goat Milk Infant Formula (Stage 1); packaged in 800g (1.8lbs) tin cans - six cans per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Little Oak Company Ltd.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 11, 2023
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Puritan Bennett Cuff Pressure Manager, REF: 180-03
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien
FDA (openFDA device enforcement)
Reported Oct 11, 2023
therascreen ¿KRAS RGQ PCR Kit (24)-IVD qualitative PCR assay used on the Rotor-Gene Q MDx instrument for the detection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen GmbH
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Heartmate 3 LVAS Implant Kit, REF: 106524US, 106524INT; Heartmate XVE & HeartMate II Apical Coring Knife, REF: 1050
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
2 oz VIVE ORGANIC DETOX + IMMUNITY KIWI APPLE SUPERGREENS WELLNESS SHOT; Total package size: 12 bottles per case;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vive Organic
FDA (openFDA food enforcement)
Reported Oct 4, 2023
Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
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.