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 Jul 15, 2020

TOMTEC-ARENA TTA2;software version no. 2.20 and lower; Picture archiving and communications system. Software Versions…

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

Tomtec Imaging Systems GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Jul 15, 2020

VistaSolution, physiological signal transmitter. A software graphical user interface for use by healthcare…

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

Vitalconnect Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2020

Flow Coupler Monitor, GEM, Global Excellence Microsurgery, Rx Only

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2020

CODAN SWAN-LOCK Swabable Needlefree Connector, Catalog #BC1000N, REF 16.7220, individually packaged, 504/case, Sterile.…

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

Codan US Corporation

FDA (openFDA device enforcement)

Food

Reported Jul 8, 2020

Simply Nature Sweet Potato Bites, 12oz retail boxes variety pack, Expiration date 4/9/2022. Lot code R20AJ-01A.

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

Dr. Praeger's Sensible Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 8, 2020

Leksell Vantage Stereotactic System, UDI/GTIN 7340048304887

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

Elekta Instrument AB

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2020

Elekta Unity, Image-Guided Radiation Therapy System

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2020

Control Panel REF - 60-02-50: LivaNova SCP Pump Control Panel S5/C5. REF 60-02-50, IPX2, RxOnly, UDI: 04033817900993

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

LivaNova Deutschland GmbH

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2020

Sterile Disposable Connectors ASY CONN Y 1/2X1/2X3/8 STR 24. REF/ GTIN for Insert Label:029165000/ 00803622123153

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

LivaNova USA Inc.

21 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2020

ABL80-FLEX-393-839 Box Label, REF 393-839, IVD, CE, UDI: 05700693938394 - Product Usage: It is intended for use in a…

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

Radiometer Medical ApS

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 8, 2020

TOUFAYAN BAKERIES SMART POCKETS EVERYTHING 6 COUNT NET WT 7.4 OZ. (210 g), UPC 0 7312400792 7. 12 packages per case.…

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

Toufayan Bakery, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2020

BioPince Full Core Biopsy Instrument 16ga x 15cm.,Use with Optional CO-Axial Needle MCXS1615BP. QTY.: 5/CS - Product…

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

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 1, 2020

Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD ; 30004 LokomatPro L6.2 120V Kombi; 30005 LokomatPro L6.2…

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

Hocoma AG

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2020

"Radhuni Curry Powder, 400 grams (14.11 oz.)***Ingredients: Coriander, Tumeric, Chili, Bitsalt, Aniseed, Sodium…

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

New Hoque & Sons, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2020

Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint…

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

Providence Medical Technologies

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2020

Xi Zhi Liang Fruit Jelly Cups; 21.1oz (600g); packaged in pink, yellow, and blue plastic backpacks with numerous…

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

Rong Shing Trading NY Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2020

Atellica Solution IM1300 Analyzer, Siemens Material Number 11066001, UDI # 00630414007960

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

Siemens Healthcare Diagnostics, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2020

Stumptown Cold Brew Coffee and Chocolate with Oatmilk. Product is TetraPak Prisma Pak aseptic packaging. Keep…

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

Stumptown Coffee Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2020

Oscar 2, Model 250 System

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

Suntech Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2020

Alinity C, Processing Module. Chemistry analyzer for in-vitro diagnostics.

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2020

PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only STERILE EO - Product Usage: The Biosense Webster…

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

Biosense Webster

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2020

Leica ARveo and M530 OH6 microscope systems.

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2020

VITROS Chemistry Product AMYL Slides Reagent, AMYLASE/5 PACK/300 SLDS, Product Code 1202670, UDI # 10758750008513 -…

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

Ortho-Clinical Diagnostics

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2020

BD FACS Sample Prep Assistant (SPA) II - Product Usage: K050191: The BD FACSCanto system with BD FACSCanto clinical…

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

Becton, Dickinson and Company, BD Biosciences

2 more products 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.