The Recall Desk

State

New York product recalls

72,982 recalls have nationwide distribution and so reach New York. 12,905 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,905
Critical
1,501
Severe
3,135
Most recent
2026-09-16

Of the 12,905 recalls naming New York we have scored against our rubric, 1,501 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,135 (24%) are Severe.

These figures cover only the 12,905 recalls whose distribution notice names New York specifically. The 72,982 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6501–6525 of 85887

  • SevereFDA (Food)·H-0215-2025·2025-07-16

    Weaver bulk semi-sweet chocolate nonpareils recalled over undeclared milk allergen

    Weaver Chocolates Nonpareil Semi-Sweet Chocolate in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 849 cases are affected.

    Product
    Weaver Chocolates, 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds) - 25 lbs. Bulk Cases
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Devices)·Z-2081-2025·2025-07-16

    Optisite OPTI18 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI18 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 13,240 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI18 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorpo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0216-2025·2025-07-16

    Weaver white seed nonpareil chocolate recalled over undeclared milk allergen

    Weaver Chocolates Nonpareil Semi-Sweet Chocolate (White Seeds) in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 1,760 cases are affected.

    Product
    Weaver Chocolates, D2645 - Nonpareil, Semi-Sweet Chocolate (White Seeds) - 25 lbs. Bulk Cases
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Devices)·Z-2084-2025·2025-07-16

    FEM-FLEX II FEMII018A cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 13,240 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2047-2025·2025-07-16

    Bravo CF capsule delivery devices may have misapplied adhesive causing malfunction

    The Bravo CF capsule delivery device is being recalled because misapplied adhesive may prevent the pH capsule attaching to the oesophagus or detaching from the delivery device. 128,202 units affected.

    Product
    Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V470000·2025-07-16

    BMW electric vehicle battery modules may be improperly assembled

    BMW is recalling certain 2022-2025 iX, 2023-2024 i7 and 2022-2023 i4 vehicles because high-voltage battery cell modules may not have been assembled properly, stressing the module frame.

    Product
    BMW — BMW I4, I7, IX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0278-2025·2025-07-16

    Wegmans semi-sweet chocolate nonpareils recalled over undeclared milk allergen

    Wegmans Semi-Sweet Chocolate Nonpareils are being recalled because of undeclared milk. 595 cases are affected across nine states and the District of Columbia.

    Product
    Wegmans Semi-Sweet Chocolate Nonpareils, NET WT 18.5 OZ (1 LB 2.5 OZ) (524 g), packaged in a plastic tub and packed 12 per case, Distributed by: Wegmans Food Markets, Inc. Rochester, NY 14603. Ingredients: Sugar, Chocolate Liquor, Cacao Fat, Corn Starch, Soy Lecithin (emulsifier
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0219-2025·2025-07-16

    Wegmans French toast mini muffins may contain foreign objects of metal

    Wegmans brand French Toast Mini Muffins are being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.

    Product
    a. Wegmans brand Mini Muffins; FRENCH TOAST; NET WT 22 OZ (1 LB 6 OZ) 624 g; FAMILY PACK; packaged in plastic clamshell; UPC 7789058612 b. Wegmans brand Mini Muffins; FRENCH TOAST; NET WT 13 OZ (369 g); packaged in plastic clamshell; UPC: 7789052435
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0220-2025·2025-07-16

    Wegmans chocolate chip mini muffins may contain foreign objects of metal

    Wegmans brand Chocolate Chip Mini Muffins are being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.

    Product
    Wegmans brand Mini Muffins; CHOCOLATE CHIP; NET WT 13.5 OZ; packaged in plastic clamshell; UPC 7789053223
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2104-2025·2025-07-16

    VersaCross RF wire lots may have a punctured sterile barrier pouch

    The VersaCross RF Wire is being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units are affected.

    Product
    VersaCross RF Wire (VXW). Indicated for creation of an atrial septal defect in the heart. Product ID VXW0002 Device approved and commercialized in Japan only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2097-2025·2025-07-16

    Infinia nuclear medicine systems may show unintended radial detector motion

    Infinia, Infinia Hawkeye, Infinia II and Infinia II Hawkeye 4 nuclear medicine systems are being recalled because unintended radial detector motion may occur without the correct gantry software. 1,822 units affected.

    Product
    Infinia, Infinia Hawkeye, Infinia II, Infinia II Hawkeye 4 Nuclear Medicine system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2101-2025·2025-07-16

    O-arm O2 imaging system gantry support may have been damaged

    The O-arm O2 Imaging System is being recalled because a mechanical component supporting the gantry to the support structure may have been damaged during manufacture. 3 units affected.

    Product
    O-arm O2 Imaging System. Mobile X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2108-2025·2025-07-16

    Alcon Constellation vitrectomy packs may have damaged lidding compromising sterility

    Alcon Constellation Vision System Vitrectomy Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 198,205 units affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constella
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2103-2025·2025-07-16

    VersaCross access kits may have a hole in the sterile pouch

    VersaCross Access Solution kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    VersaCross Access Solution (VXSK), Product Description and ID: VXSK (180J RF WIRE 63CM/45DEG/D0) VXSK0101 VXSK (180J RF WIRE 63CM/45DEG/D1) VXSK0102 VXSK (180J RF WIRE 63CM/55DEG/D0) VXSK0103 VXSK (180P RF WIRE 63CM/45DEG/D0) VXSK0121 VXSK (180P RF WIRE 63CM/45DEG/D1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2105-2025·2025-07-16

    VersaCross transseptal sheath kits may have a punctured sterile barrier pouch

    VersaCross Transseptal Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS 63CM/45DEG/D0 SHEATH VXS2112 VERSACROSS SHEATH (63CM 45DEG D0)-J Used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, includ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2106-2025·2025-07-16

    Torflex transseptal guiding sheath kits may have a punctured sterile pouch

    Torflex Transseptal Guiding Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F 63CM 45DEG TF85-32-63-55 TORFLEX 8.5F 63CM 55DEG Used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, including the left atri
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2109-2025·2025-07-16

    Alcon Constellation procedure packs may have damaged lidding compromising sterility

    Alcon Constellation Vision System Combined Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 89,495 units affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Combined Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constellati
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0218-2025·2025-07-16

    Wegmans blueberry mini muffins may contain foreign objects of metal origin

    Wegmans brand Blueberry Mini Muffins family pack is being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.

    Product
    Wegmans brand Mini Muffins; Blueberry; NET WT 20 OZ (1 LB 4 OZ) 567 g; FAMILY PACK; packaged in plastic clamshell; UPC 7789053227
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2110-2025·2025-07-16

    Alcon Custom Pak surgical kits may have damaged lidding compromising sterility

    Alcon Custom Paks, customer-designed sterile surgical kits, are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 15,557 kits affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Custom Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Alcon Custom Paks are customer-designed sterile surgical procedure packs / convenience kits intende
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2098-2025·2025-07-16

    Nuclear medicine systems may show unintended radial detector motion during scans

    Varicam, Millennium VG, Millennium VG Hawkeye and Discovery VH nuclear medicine systems are being recalled because unintended radial detector motion may occur without the correct gantry software version. 21 units affected.

    Product
    Varicam, Millennium VG, Millennium VG Hawkeye, Discovery VH Nuclear Medicine System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0252-2025·2025-07-16

    Calais grape jelly contains undeclared FD&C Blue 1 and Red 40

    Calais brand Grape Jelly in 1 gallon containers is being recalled because it contains undeclared colours FD&C Blue 1 and FD&C Red 40. 43 cases are affected.

    Product
    Calais Brand Grape jelly; 128 FL. OZ. (1 GAL.) 3.785 L; INGREDIENTS: Grape Juice, Corn Syrup, High Fructose Corn Syrup, Pectin, Citric Acid; REFRIGERATE AFTER OPENING; UPC 040264 10128 0
    Category
    Food
    Distribution
    2 states