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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.

Medical devices

Reported Feb 12, 2020

Reinforced Introducer Sets Maquet 7 Fr., Part Number: 0684 00 0403 06. It is an accessory to be used for percutaneous…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Datascope Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Ducktrap River of Maine Herring Center Cuts in Wine Sauce, 12 oz.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Ducktrap River

FDA (openFDA food enforcement)

Food

Reported Feb 12, 2020

Garlic Parmesan Sauce; DP# 4478 FG# 02620 8/16 fl. oz (4.73 ml) pouches; NET WT. 8.05 lbs (3.65 kg) Produced for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Golden State Foods

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

da Vinci Xi Surgical System Surgical System, IS4000, 00886874114216 - Product Usage: used with an endoscope, surgical…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2020

Vaginal Verification Panel Ref 8208 Lot 8208-11

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microbiologics Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Munk Pack Keto Nut and Seed Dark Chocolate Sea Salt Bar, 35 g, individual unit

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Munk Pack Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pacific Medical Group Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2020

PediaLift Access Device, Device Identifier: B751PDLFT0

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

PediaLift LLC

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

QUESOS LA RICURA brand Queso Cotija; Cotija Cheese; AGED OVER 60 DAYS; Ingredients: Raw Milk, Salt, Enzyme and…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Quesos La Ricura, Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Liquid Clinical Chemistry Control, Catalogue Number: LAE4217, Size: 12 x 5 ml

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Randox Laboratories Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

GIBSON Healthcare Membrane 6-9, 15mm x 20mm, Reference Number 5303-226 - Product Usage: Indicated for use in oral…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Collagen Matrix Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2020

Excellent tahina (sesame tahini) 800 g and 400 g jars, UPC 6214002717420 and 6214002717413

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Five Star Food Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2020

CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Haemonetics Corporation

21 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

The da Vinci SP surgical system is made of three main components: the Surgeon Console (SC), the Vision Cart (VC), and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2020

Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Jeni's Splendid Ice Creams LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2020

Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Johnson & Johnson Surgical Vision Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2020

kindroot adaptogems; Peach Blossom Plant lozenges for lit looks. 20 lozenges net wt. 2.6 oz. 74 g - Dietary Supplement…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Kindroot LLC

FDA (openFDA food enforcement)

Drugs

Reported Feb 5, 2020

Dimercaptopropanesulfonate Sodium (DMPS), Aqueous injection solution, 50mg/mL 5 mL SDV, Rx only, McGuff Compounding…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

McGuff Compounding Pharmacy Services, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 5, 2020

AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

Cobas infinity central lab / cobas infinity core license-a Calculator/Data Processing Module, For Clinical Use Material…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2020

TruDi NAV Suction, TDNS000Z, 0 Degree Tip Angle, (01)10705031245877

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Acclarent, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2020

VACUETTE TUBE, 3.5mL CAL Serum Sep Clot Activator, REF 454067P - Product Usage: VACUETTE Tubes, Holders, and Needles…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Greiner Bio-One North America, 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.