The Recall Desk

State

New York product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49001–49025 of 86780

  • HighFDA (Devices)·Z-3061-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans Filtron 250 Due to Seal Integrity

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 250 because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans Filtron 250, 3-TT-FILTRON 250. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3052-2017·2017-08-30

    Medtronic Curved Suction 70 Recalled for Verification Failure

    Medtronic is recalling 149 Curved Suction 70 ENT instruments because they fail required pre-use verification checks.

    Product
    Medtronic Curved Suction 70 9733450 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3063-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans Filtron 1000 Due to Seal Integrity

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 1000 because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans Filtron 1000, 3-TT-FILTRON 1000. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3437-2017·2017-08-30

    Penobscot McCrum Recalls Seasoned Jo-Jo Wedges for Undeclared Milk

    Penobscot McCrum LLC is recalling Extra Large Seasoned/Battered Jo-Jo Wedges because the product may contain undeclared milk.

    Product
    Extra Large Seasoned/Battered Jo-Jo Wedges / 00148 (5 lb bags)
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-3048-2017·2017-08-30

    Solta Medical Recalls VASER PRO Amplifiers Due to Burn Risk

    Solta Medical is recalling seven VASER PRO Amplifiers because a service depot repair may have caused inaccurate calibration, posing a risk of patient burns.

    Product
    VASER PRO Amplifier, VASER 2.2 VASERlipo System stem, Rx Only, 115/230V - 60/50Hz 300VA The Vaser amplifier is intended for the fragmentation and emulsification of subcutaneous fatty tissues for aesthetic body contouring (modification of the anatomy).
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-3064-2017·2017-08-30

    FDA Recalls Tissu-Trans Filtron 2000 Due to Sterile Seal Integrity Concerns

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 2000 because the sterile package seal integrity cannot be assured.

    Product
    Tissu-Trans Filtron 2000, 3-TT-FILTRON 2000. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3438-2017·2017-08-30

    Valero Baby Wedges Recalled for Undeclared Milk

    Penobscot McCrum LLC is recalling Valero Baby Wedges with Crisp Coat UC Coating because the product may contain undeclared milk.

    Product
    Valero Baby Wedges with Crisp Coat UC Coating / 51049 (5 lb bags)
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-3065-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans MEGA 1500 Due to Seal Integrity

    Shippert Medical Technologies is recalling Tissu-Trans MEGA 1500 devices because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans MEGA 1500, 3-TT-MEGA 1500. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3453-2017·2017-08-30

    Wegmans Apple Cranberry Crostata Recalled for Undeclared Soy Lecithin

    Wegmans is recalling Apple Cranberry Crostata products because they contain undeclared soy lecithin. The products were sold in New York, New Jersey, Massachusetts, Virginia, and Maryland.

    Product
    Wegmans Apple Cranberry Crostata, Large, Net Wt. 23 oz. and 6 oz.. (In-Store Bakery)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-3454-2017·2017-08-30

    Wegmans Nectarine Crostata Recalled for Undeclared Soy Lecithin

    Wegmans Food Markets is recalling Nectarine Crostata products due to undeclared soy lecithin, a potential allergen hazard.

    Product
    Wegmans Nectarine Crostata, Large, Net Wt. 23 oz. and 6 oz.. (In-Store Bakery)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-3058-2017·2017-08-30

    Medtronic ENT Navigation Suction Devices Recalled for Verification Failure

    Medtronic Navigation is recalling six kits of ENT suction devices because they fail required pre-use verification checks.

    Product
    Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM, reusable, Rx. This kit includes 9733908 (which includes 9733452 containing 9733449, Straight Suction, 9733450, 70 deg Curved Suction, and 9733451, 90 deg Curved Suction). The firm name on the label is Medtronic Navigation, Inc.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3441-2017·2017-08-30

    Penobscot McCrum Recalls Battered Jo-Jo Wedges for Undeclared Milk

    Penobscot McCrum LLC is recalling Medium Battered Jo-Jo Wedges because the product may contain undeclared milk, posing a risk to individuals with milk allergies.

    Product
    Medium Battered Jo-Jo Wedges / 00126 (5 lb bags)
    Category
    Food
    Distribution
    26 states
  • HighNHTSA·17V539000·2017-08-30

    New Flyer Transit Bus Seat Belt Buckle Recall

    New Flyer is recalling 2015-2017 transit buses because the driver's seat belt buckle may be stuck, preventing the belt from latching.

    Product
    NEW FLYER — NEW FLYER MD30, XD40, XN40, MD35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3442-2017·2017-08-30

    Fairway Cookies Blondie Recalled for Undeclared Walnuts

    Fairway Group Holdings Corp is recalling 323 units of Cookies Blondie due to undeclared walnuts. The product was distributed in New York, New Jersey, and Connecticut.

    Product
    Fairway brand Cookies Blondie, 10 oz. Item Code 268492 XXXXXX or 263413 XXXXXX.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-3069-2017·2017-08-30

    Medtronic Recalls Deep Brain Stimulation Lead Kits Due to Depth Stop Defect

    Medtronic is recalling Deep Brain Stimulation lead kits because the depth stop may not secure properly, potentially causing the lead to be placed beyond the intended target.

    Product
    DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and 3391/3391S, The lead kit contains one DBS lead in addition to multiple accessories used in DBS lead implant procedures. Among these accessories is the DBS lead…
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Food)·F-3409-2017·2017-08-30

    Grandma's Herbs Cholesterol Support Recalled for Undeclared Soy Lecithin

    Grandma's Herbs is recalling Cholesterol Support dietary supplements because they contain undeclared soy lecithin, a common allergen.

    Product
    "Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT, Dietary Supplement, 100 Capsules 480 mg. Packaging: PET plastic bottles, UPC# 714938 00046
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17215·2017-08-30

    Dr. Brown's Natural Bottle and Dish Soap Recalled for Bacteria Risk

    Handi-Craft is recalling Dr. Brown's Natural Bottle & Dish Soap because it may contain harmful bacteria. No injuries have been reported.

    Product
    Dr. Brown's Natural bottle and dish soap
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3051-2017·2017-08-30

    Medtronic ENT Suction Devices Recalled for Verification Failure

    Medtronic Navigation is recalling 277 reusable ENT suction instruments because they fail pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.

    Product
    Medtronic Straight Suction 9733449 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3050-2017·2017-08-30

    Alcon ORA System Recall for Incorrect IOL Power Measurements

    Alcon is recalling 367 ORA Systems with VerifEye because a software error may cause incorrect intraocular lens power measurements during cataract surgery.

    Product
    ORA System with VerifEye, Catalog Number 8065998300 For use during intraocular lens surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3060-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans Filtron 100 Due to Seal Integrity

    Shippert Medical Technologies is recalling Tissu-Trans Filtron 100 units because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans Filtron 100, 3-TT-FILTRON 100. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3452-2017·2017-08-30

    Wegmans Apple Crostata Recalled for Undeclared Soy Lecithin

    Wegmans is recalling Apple Crostata products due to undeclared soy lecithin, a potential allergen hazard for sensitive consumers.

    Product
    Wegmans Apple Crostata, Large, Net Wt. 23 oz. and 6 oz. (In-Store Bakery)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-3455-2017·2017-08-30

    Wegmans Peach Crostata Recalled for Undeclared Soy Lecithin

    Wegmans Food Markets is recalling Peach Crostata products due to undeclared soy lecithin. The products were sold in New York, New Jersey, Massachusetts, Virginia, and Maryland.

    Product
    Wegmans Peach Crostata, Large, Net Wt. 23 oz. and 6 oz.. (In-Store Bakery)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-3433-2017·2017-08-30

    Penobscot McCrum Recalls Battered Jo-Jo Wedges for Undeclared Milk

    Penobscot McCrum LLC is recalling Battered Jo-Jo Wedges because the product may contain undeclared milk, posing a risk to individuals with milk allergies.

    Product
    Battered Jo-Jo Wedges / 00047 (5 lb bags)
    Category
    Food
    Distribution
    26 states