All recall categories

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 Mar 4, 2020

Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No.…

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

Zimmer Surgical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2020

DP-30 Digital Ultrasonic Diagnostic Imaging System, Part No. 1155E-PA00004 - Product Usage: The Digital Ultrasonic…

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

Mindray DS USA, Inc. dba Mindray North America

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2020

SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx…

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

Ormco/Sybronendo

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2020

CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic,…

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

Philips Medical Systems GmbH, DMC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2020

Philips HeartStart FRx AED, Model 861304, FRx codeRev: E.02.017

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

Philips North America LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 26, 2020

Suja Organic Berry Zest Fruit + Veggie Smoothie, 12 oz. UPC: 81861702234

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

Suja Life LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 26, 2020

OPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 05051700017565

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

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

Bakers Corner All Purpose Flour in 5 lb. bags

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

Adm Milling

18 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B

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

Arrow International Inc.

48 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Feb 19, 2020

Kushim Tablets (Gushim) 45-count packages, Label in foreign language

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

B and a Trading Corporation

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 19, 2020

SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115. The product is a femoral cutting block.

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

Yossef Roasting Co. Handcrafted Nuts Watermelon Seeds; 7oz.

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

IL Nuts

FDA (openFDA food enforcement)

Food

Reported Feb 19, 2020

bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc.,…

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

Market America Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…

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

Medtronic Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot…

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

Nextremity Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…

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

Pacific Medical Group Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

Ready Pac Bistro - Spinach Dijon Salad with Sweet Onion Dijon Vinaigrette; Baby Spinach, Hard Boiled Eggs, Monterey…

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

Ready Pac Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

cobas infinity core, Material No. 7154003001. The device is a calculator/data processing module, for clinical use.

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Double-Double, REF 3910-500-472, UDI 07613327464832, Sterile R,…

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

Stryker Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

Granulate Pure Cane Sugar sold under the brand names of: Ahold 16 oz canister, DISTRIBUTED BY FOODHOLD USA, LLC,…

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

Sugar Foods Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

Terumo Advanced Perfusion System 1 Roller Pump, 4 Inch, Catalog Number 816570 - Product Usage: is indicated for use for…

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

Terumo Cardiovascular Systems Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Bulk Pail Product -- Almark Foods HARD COOKED BROKEN EGG WHITES 20 LB pail, DIST BY: ALMARK FOODS, GAINESVILLE, GA…

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

Almark Foods, LLC

28 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Cocoon Convective Warming System, Product Code: CWS4000 (110V).

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

Care Essentials Pty., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Catsmo brand Gold (sliced, whole, 4oz); Scottish (Whole, Sliced, Whole No Skin, 1lb, 4oz); Loin; Organic (4oz); Double…

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

Catsmo LLC

6 more products in this recall

FDA (openFDA food 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.