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 Jun 8, 2022
Jason & Mary Large Milk Peanut Butter Cup
High riskUsing this product could cause serious injury, illness or death — stop using it now.Walnut Creek Chocolate Co. Inc.
14 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2022
Wegmans Food You Feel Good About Lobster Bisque - 16 oz packaged in a 4 x 4 x 3.75" clear plastic tub with a snap on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
FDA (openFDA food enforcement)
Reported Jun 8, 2022
XVIVO Organ Chamber REF 19020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xvivo Perfusion Ab
FDA (openFDA device enforcement)
Reported Jun 1, 2022
SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market unit contains 10 individual wafers.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Jun 1, 2022
HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Devicor Medical Products Inc.
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System; The device is placed in a plastic tray with a snap on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Wegmans Brand Fresh Goat Cheese, Classic Chevre, with Cranberries, 5.5lb; packaged in Cryovac Bags
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Old Chatham Sheepherding Creamery, LLC
FDA (openFDA food enforcement)
Reported Jun 1, 2022
(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
AC-powered adjustable medical beds with built-in electric DC actuators and controls.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Umano Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 25, 2022
Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Vascular
FDA (openFDA device enforcement)
Reported May 25, 2022
MicroScan WalkAway-40 plus Instrument REF B1018-283
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 25, 2022
BioPlex 2200 REF 12000670 ToRC IgM Reagent Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
VITRIGUARD, CARRIER, CLEAR; Model. No. 43782001 The VitriGuard device is a cryopreservation storage device composed of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
Getinge 9100-Series Washer Disinfector models: 9120E, 9125E, 9127E, 9128E, 9122EW, 9128EW.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
Gorton s Fish Sandwich Fillets, 18.3 OZ, UPC 44400 15440
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gorton's, Inc.
FDA (openFDA food enforcement)
Reported May 25, 2022
Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin. Not for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported May 25, 2022
Yes! Enoki Mushrooms; Pesticide Free Produce: Vacuumed packed. Product of China UPC: 825382736947 Net Wt 200g/7.05 oz…
High riskUsing this product could cause serious injury, illness or death — stop using it now.T Fresh Company dba Yes Produce
FDA (openFDA food enforcement)
Reported May 25, 2022
Total Resources International First Aid Kits, Item Numbers: 10HBC01087, 10HBC01092A3PK, 10HBC01112, 10HBC01113,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Total Resources Intl
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 25, 2022
Turbett Surgical Container, TS1500
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Turbett Surgical, LLC
FDA (openFDA device enforcement)
Reported May 18, 2022
putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cerapedics, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Certified Safety Mfg Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Daavlin Distributing Company
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.