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 48,100 notices were distributed nationwide, so they reach New York too — those are in the archive.
Reported Aug 9, 2023
NanoZoomer S360MD Slide scanner system-automated system for creating, viewing, and managing digital slides. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamamatsu Corporation
FDA (openFDA device enforcement)
Reported Aug 9, 2023
VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2023
NeuMoDx Cartridge-used for extraction, purification, amplification and detection of nucleic acids on the NeuMoDx 288…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NeuMoDx Molecular Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2023
Zimmer Periarticular Locking Plate (ZPLP) Distal Lateral Femoral Plate 6 holes 159 mm Length-Indicated for temporary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Aug 2, 2023
HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2023
FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microvention Inc.
FDA (openFDA device enforcement)
Reported Aug 2, 2023
SPRING VALLEY brand POTATO BLINTZES; NET WT. 13 OZ (369g); KEEP FROZEN; READY TO COOK; INGREDIENTS: WHEAT FLOUR (WHET…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Milmar Food Corp.
FDA (openFDA food enforcement)
Reported Aug 2, 2023
QIAstat-Dx¿ Respiratory SARS-CoV-2 Panel -IVD intended for the detection and differentiation of nucleic acid from…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2023
Cios Select VA 21 with FD- A Mobile X-ray system intended for use in Operating room, Traumatology, Endoscopy, Intensive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Contour¿ next GEN Blood Glucose Monitoring System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascensia Diabetes Care US, Inc.
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical GmbH
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Aeris Balloon Dilation Catheter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bryan Medical Inc.
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Simplexa Direct Amplification Disc Kit, Rx Only, IVD The Simplexa Direct Amplification Disc Kit, REF: MOL1455 is 1 box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Digisonics, Inc.
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Jul 19, 2023
Tampico brand Mango Punch; LESS THAN 1% JUICE; 1 GAL (3.78 L); INGREDIENTS: WATER, HIGH FRUCTOSE CORN SYRUP, LESS THAN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Garelick Farms LLC
FDA (openFDA food enforcement)
Reported Jul 19, 2023
HeartSine, REF: PAD-PAK-01, PAD-PAK-03 AND PAD-PAK-03j, CE0123 sold separately and with the HeartSine Samaritan Public…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Jul 19, 2023
Great Value Sliced Strawberries. Item # 107356. Frozen, packaged flexible plastic bags. Net wt. 4 lbs (64oz). UPC on…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oregon Potato Company
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 19, 2023
REF: 218-1604, 1.6mm x 4mm Profile Zero Auto-Drive Screw, Rx Only, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Osteomed, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 12, 2023
Maggi Masala ae Magic, 6 grams, Packaged in plastic sachets. 1920 sachets per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amin Trading Agency LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 12, 2023
BD Synapsys Informatics Solution, Catalog Number 444150
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
Cricket Creek Farm brand Sophelise cheese
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cricket Creek Farm LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 12, 2023
da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
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.