The Recall Desk

State

New York product recalls

73,809 recalls have nationwide distribution and so reach New York. 12,956 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,956
Critical
1,508
Severe
3,702
Most recent
2026-11-04

Of the 12,956 recalls naming New York we have scored against our rubric, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,702 (29%) are Severe.

These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41476–41500 of 86765

  • SevereFDA (Devices)·Z-0901-2019·2019-03-06

    Philips Ingenia MRI System Recalled Due to Ceiling Speaker Hazard

    Philips is recalling Ingenia 1.5T CX MRI systems because ceiling speakers may be pulled by the magnetic field and fall.

    Product
    Ingenia 1.5T CX, Model Number 781261. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1092-2019·2019-03-06

    Produce Packaging Inc. Recalls Veggie Rice Blend Due to E. coli Risk

    Produce Packaging Inc. is recalling 10 LB Veggie Rice Blend products due to potential E. coli contamination. The products were distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Mix, Veggie Rice Blend, 10 LB
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0918-2019·2019-03-06

    Philips Ingenia 3.0T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia 3.0T, Model Number 781377. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1107-2019·2019-03-06

    Whole Foods Spinach Ravioli Salad Recalled for Salmonella Risk

    Whole Foods Market is recalling Spinach Ravioli Salad with Lemon, Tomato, and Parmesan due to potential Salmonella contamination.

    Product
    Spinach Ravioli Salad with Lemon, Tomato, and Parmesan packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0916-2019·2019-03-06

    Philips Ingenia 1.5T S MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia 1.5T S MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia 1.5T S, Model Number 781347. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1087-2019·2019-03-06

    Produce Packaging Inc. Recalls Cauliflower Florets Due to E. coli Risk

    Produce Packaging Inc. is recalling Cauliflower, Floret 4/3 LB due to potential E. coli contamination. The product was distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Cauliflower, Floret 4/3 LB
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0885-2019·2019-03-06

    Philips Intera IT MRI Systems Recalled for Falling Ceiling Speaker Risk

    Philips is recalling 11,226 Intera IT MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera IT, Model Number 781160. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0904-2019·2019-03-06

    Philips Ingenia 3.0T CX MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia 3.0T CX MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia 3.0T CX, Model Number 781271. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0897-2019·2019-03-06

    Philips Achieva 7.0T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Achieva 7.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 7.0T, Model Number 781240. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0875-2019·2019-03-06

    Philips MRI Systems Recalled Due to Ceiling Speaker Fall Risk

    Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.0T Omni/Stellar, Model Number 781102. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0948-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that could cause leaks and reduced drug delivery.

    Product
    AF 550 x 5ML/HR 2ML 60LO CPNB, Product code MT5060XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V168000·2019-03-06

    Highland Ridge RV Recalls 2019 Travel Trailers Due to Incorrect Weight Label

    Highland Ridge RV is recalling 74 units of 2019 Mesa Ridge and Open Range Ultra Lite travel trailers because the weight label exceeds the safety chain rating.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OPEN RANGE ULTRA LITE, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0953-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International Inc. is recalling specific Arrow AutoFuser Disposable Pain Control Pumps due to possible cracks on the fill port connector that may cause leaks and reduced drug delivery.

    Product
    AF w/AS 550 x 1-14 ml/hr, 5ml30 LOCPNB, Product code MVBX30XLCPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0943-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Leaks

    Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that may cause leaks and reduced drug delivery.

    Product
    AF550x5ML/H 2ML 60LO 6" DUAL CATHS, 4.5", Product MT5060XLYK5 CP, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0952-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International is recalling 26 units of the AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.

    Product
    AF w/AS 550 x 0.5-7 ml,w/Y site,DL CPNB, Product code MVAXL2Y CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0930-2019·2019-03-06

    Philips MARLIN 1.5T MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling MARLIN 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    MARLIN 1.5T, Model Number 781474. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0920-2019·2019-03-06

    Philips Ingenia Ambition S MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Ingenia Ambition S MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia Ambition S, Model Number 781359. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0946-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International is recalling 8 units of the AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.

    Product
    AF 550 x 5ML/H 6" DUAL CATHS, 4.5", Product code MC0050XLYK5 CP, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0950-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Leaks

    Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that may cause leaks and reduced drug delivery.

    Product
    AF 550 x 8ML/HR 2ML 15LO CPNBMT8015XL CP, Product code MT8015XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0874-2019·2019-03-06

    Philips Intera 0.5T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Intera 0.5T MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Intera 0.5T Standard, Model Number 781101. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide