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 48,100 notices were distributed nationwide, so they reach New York too — those are in the archive.

Medical devices

Reported May 15, 2024

Intelli-C: Right side suspended Tabletop, REF: 03400000; Left side suspended Tabletop, REF: 03400010, used with the…

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

Nrt X-Ray A/s

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2024

5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/795143, 5500 W/795144, 5500 G/795145, and…

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

Philips Ultrasound, Inc.

FDA (openFDA device enforcement)

Food

Reported May 15, 2024

Martinelli's Gold Medal Apple Juice From U.S. Grown Fresh Apples 1 Liter (33.8 fl oz.) No Additives of Any Kind UPC 0…

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

S Martinelli & Company

FDA (openFDA food enforcement)

Food

Reported May 15, 2024

Java Wafer - Mocha Hazelnut [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]

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

Sacramento Cookie Factory

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 8, 2024

Abbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,

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

Allergan Sales, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Medtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100, REF: PMAC71RIC

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

Covidien

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 8, 2024

King Kullen Broccoli Cutlets with Breadcrumbs and Parmesan; 20oz; oven safe tin package with a clear dome top marked…

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

Gracie's Kitchens Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 8, 2024

INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup

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

Innomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test Chamber 21 Gauge REF OPOHF21L The…

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

Johnson & Johnson Surgical Vision, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly

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

Thoratec Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

3M Durapore Surgical Tape, Catalog Number 1538-118

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga Chang Hydrodissection Cannulas. These Custom…

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported May 1, 2024

Amy's Kitchen Enchilada Verde Whole Meal 10 oz. 12 pk Item # 000085

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

Amy's Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 1, 2024

Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and pelvic surgery

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.

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

Parker Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests

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

Quidel Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Route 92 Medical Full Length 070 Access System, REF 7002, Rxonly, SterileEO. Used for Introduction of interventional…

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

Route 92 Medical Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System,…

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

Siemens Medical Solutions USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Apr 26, 2024

802 VT Frozen Recalls Frozen Meat Pizza Products Due to Misbranding and Undeclared Allergens

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

VT Pie and Pasta Co.

USDA FSIS

Food

Reported Apr 24, 2024

Aromitalia Malasia Coconut Paste + 35.27 oz milk-based mix, Net Weight 123.46 oz, plastic container.

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

Aromitalia USA Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 24, 2024

Tranquility & Teachings William Monague plate set, brand Indigenous Collection by CAP. Each box consists of two plates,…

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

Canadian Art Prints

FDA (openFDA food enforcement)

Medical devices

Reported Apr 24, 2024

STRATAFIX Spiral MONOCRYL Plus Bidirectional Knotless Tissue Control Device: STRATAFIX SPIRAL MONOCRYL PLUS BI UD…

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

Ethicon, 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.