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

In the agency's Nov 11, 2026 enforcement report

Hemochron Jr., Whole Blood Microcoagulation System, Activated Partial Thromboplastin Time (APTT) Test Cuvette, REF: J103

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

Accriva Diagnostics, Inc.

FDA (weekly enforcement report)

Medical devices

In the agency's Nov 11, 2026 enforcement report

Generic Name: Edwards Commander M Delivery System Generic Name: Edwards Commander M Delivery System Model/Catalog…

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

Edwards Lifesciences, LLC

FDA (weekly enforcement report)

Medical devices

In the agency's Nov 11, 2026 enforcement report

Nextseq 550Dx Instrument REF: 20005715, FOR IN VITRO DIAGNOSTIC USE

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

Illumina, Inc.

2 more products in this recall

FDA (weekly enforcement report)

Medical devices

In the agency's Nov 11, 2026 enforcement report

EVOS 3.5MM LATERAL PROXIMAL TIBIA PLATE 6 HOLE LEFT 91MM REF72463106

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

Smith & Nephew, Inc.

FDA (weekly enforcement report)

Medical devices

In the agency's Nov 11, 2026 enforcement report

Tandem Mobi Insulin Pump, Models: 1004004, 1010750, 1012676, 1012719, 1013655, 1013656, 1013501, 1013700, 1014081,…

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

Tandem Diabetes Care, Inc.

FDA (weekly enforcement report)

Medical devices

In the agency's Nov 4, 2026 enforcement report

EMAG system Model/Catalog Number: 418591/418591U Product Description: Nucleic acid sample preparation instrument IVD,…

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

BioMerieux SA

FDA (weekly enforcement report)

Food

In the agency's Nov 4, 2026 enforcement report

EDEN BROTHERS Broccoli Seeds - Calabrese. Sold in packets, Net Wt. 1oz pouches, UPC SVBRO111 -qb2 & 1 Pound pouches UPC…

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

Eden Brothers

FDA (weekly enforcement report)

Medical devices

In the agency's Nov 4, 2026 enforcement report

OmniaSecure Model 3930M, LEAD 3930M74 74 CM DF4 MR 3930M74 LEAD 3930M79 79 CM DF4 MR 3930M79 The Medtronic OmniaSecure"…

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

Medtronic, Inc.

1 more product in this recall

FDA (weekly enforcement report)

Medical devices

In the agency's Nov 4, 2026 enforcement report

Precision Pointer Electromagnetic (8000-050-001)

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

Stryker Leibinger GmbH & Co. KG

FDA (weekly enforcement report)

Medical devices

In the agency's Nov 4, 2026 enforcement report

Orthoscan VERSA Accessory Cart, REF: 1000-0021 and Versa Mini C-Arm System, REF: 1000-0020

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

Ziehm-Orthoscan Inc.

FDA (weekly enforcement report)

Food

Reported Oct 29, 2026Updated Nov 3, 2026

SLR Food Distribution Inc. Recalls Wise Wife Brand Ground Cinnamon Due to Elevated Lead Levels

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

SLR Food Distribution Inc.

FDA (recalls & safety alerts)

Medical devices

Reported Oct 28, 2026Updated Nov 2, 2026

PNE Lead Implant Kit REF: 1701

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

Axonics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2026Updated Nov 2, 2026

B Braun SAFSITE Injection Site, RV1000NC SAFSITE VALVE W/O EXTRA CAP. Catalog Number: 415068.

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

B Braun Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 28, 2026Updated Nov 2, 2026

Evexias Health Solutions Amino Ultra, 90-capsules, dietary supplement in white plastic bottles with blue/green/white…

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

Evexias Health Solution

FDA (openFDA food enforcement)

Food

Reported Oct 28, 2026Updated Nov 2, 2026

GEARHARTS FINE CHOCOLATES Net Wt. 4oz UPC 8 98111 00205 7; Net Wt. 8oz UPC 8 98111 00206; Gearharts Fine Chocolates…

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

Gearharts Fine Chocolates, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 28, 2026Updated Nov 2, 2026

Brand Name: VACUETTE Product Name: LH Lithium Heparin Separator Model/Catalog Number: 454008P Product Description:…

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2026Updated Nov 2, 2026

Ion Torrent Genexus Dx with software, Catalog: A40003539, which supports the Ion Torrent Genexus Dx Integrated Sequencer

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

Life Technologies Holdings Pte Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2026Updated Nov 2, 2026

Medtronic NDI Passive Spheres REF: 8801075, Sterile EO, 5/Tray 12 Pk., Rxonly

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

Medtronic Navigation, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2026Updated Nov 2, 2026

Philips Lumify Diagnostic Ultrasound System

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

Philips Ultrasound, LLC

FDA (openFDA device enforcement)

Food

Reported Oct 28, 2026Updated Nov 2, 2026

Sempio Yellow Peach; Product of Korea; NET WT. 14.10 oz. UPC: 8801005320825

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

Sempio Food Services, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 28, 2026Updated Nov 2, 2026

Xact mole marker for mammography Model/Catalog Number: M15RM

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

Solstice Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2026Updated Nov 2, 2026

Think Surgical Square Driver REF: 109126

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

Think Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 28, 2026Updated Nov 2, 2026

Trader Joe's Crispy Rice Milk Chocolate Bar; Imported from Belgium, 3- 1.75 oz bars. Package contains 3 individually…

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

Trader Joe's Company

FDA (openFDA food enforcement)

Food

Reported Oct 27, 2026Updated Nov 3, 2026

HAIFA SMOKED FISH Recalls Cold Smoked Sprats Due to Potential Health Risk

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

Haifa Smoked Fish

FDA (recalls & safety alerts)

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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.