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.

6,449 stored notices name New York, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach New York too — those are in the archive.

Medical devices

Reported Oct 21, 2026Updated Oct 26, 2026

Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2026Updated Oct 26, 2026

DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513

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

Beckman Coulter, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2026Updated Nov 2, 2026

Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel plus Model/Catalog Number:…

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

BioFire Diagnostics, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2026Updated Oct 26, 2026

NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2026Updated Oct 26, 2026

PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture, 1X18" TF-5, Product Code: N271H

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

Ethicon, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2026Updated Oct 26, 2026

Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816…

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

Ferno-Washington Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2026Updated Oct 26, 2026

HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009802028. in vitro diagnostic (OUS only)

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

Instrumentation Laboratory

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2026Updated Oct 26, 2026

JenaValve Trilogy Delivery Catheter, Size 27MM REF: TRILOGY-DC-L

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

Jenavalve Technology Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 21, 2026

Made Fresh brand 4 Bean Salad; 5lb white plastic tub

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

Made Fresh Salads Inc.

FDA (weekly enforcement report)

Medical devices

Reported Oct 21, 2026Updated Oct 26, 2026

MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, REF: OPRO-101; MAS Omni IMMUNETM PRO Liquid…

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

Microgenics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2026Updated Oct 26, 2026

The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Food

Reported Oct 21, 2026Updated Oct 26, 2026

Stewarts Shops Vanilla Heavenly Medley 1/2 Gallon (1.89 L), UPC Codes: 0 82086 44371 1

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

Stewart's Shops Corp.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 15, 2026

Family Farmstead Dairy Announces Recall of Raw Mild Cheddar Cheese Due to Potential E. coli O157:H7 Contamination

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Family Farmstead Dairy

1 more product in this recall

FDA (recalls & safety alerts)

Food

Reported Oct 14, 2026Updated Oct 20, 2026

Lemon Blueberry Loaf packaged in a cardboard box; Ingredients: King midas flour, Veribest pastry flour, Granulated…

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

J K Patisserie & Bakery LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Product…

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version:…

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

Nihon Kohden America LLC

FDA (openFDA device enforcement)

Food

Reported Oct 14, 2026Updated Oct 20, 2026

28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero.

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

Pepsico Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model…

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

Philips Medical Systems

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;

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

Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

Battle Bandage, REF: 32-700; Patrol IFAK Bag, Black - Advanced, REF: 81-125-BL; Patrol IFAK Bag, Multicam - Advanced,…

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

Safeguard US Operating LLC

FDA (openFDA device enforcement)

Food

Reported Oct 9, 2026Updated Nov 4, 2026

Krasnyi Oktyabr Inc. Recalls Starfish Seafood Premium Cold Smoked Norwegian Salmon Sliced (227g/8oz) Because of Possible Health Risk

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Krasnyi Oktyabr Inc.

1 more product in this recall

FDA (recalls & safety alerts)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part:…

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

Alere San Diego, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Oct 7, 2026

Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced

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

American National Red Cross (the)

FDA (weekly enforcement report)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 18) WHITE Model/Catalog Number:…

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

ASP Global, LLC.

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.