The Recall Desk

State

New Jersey product recalls

72,984 recalls have nationwide distribution and so reach New Jersey. 9,760 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,760
Critical
1,249
Severe
2,483
Most recent
2026-09-16

Of the 9,760 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,483 (25%) are Severe.

Which agencies issued them

These figures cover only the 9,760 recalls whose distribution notice names New Jersey specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6426–6450 of 82744

  • 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 (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-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-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
  • 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-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-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 (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-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 (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 (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
  • ModerateFDA (Food)·H-0235-2025·2025-07-16

    Organic bok choy recalled over possible reach truck fluid contamination

    Organic bok choy and organic baby bok choy are being recalled because they may be contaminated with fluid from a reach truck. The action covers 213 cases in total.

    Product
    1. USA ORGC BOK CHOY 2. USA/MEX OG2 BABY BOKCHOY
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0509-2025·2025-07-16

    Famciclovir tablets recalled after a hair was found on a tablet

    Famciclovir Tablets USP 500 mg from Macleods Pharma are being recalled because a black hair strand was found attached to a tablet in a sealed bottle. 9,888 bottles are affected.

    Product
    FAMCICLOVIR — FAMCICLOVIR (FAMCICLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0242-2025·2025-07-16

    Organic leaf lettuce and romaine recalled over reach truck fluid contamination

    Organic red leaf lettuce, green romaine, butter lettuce and living butter lettuce are being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.

    Product
    1. CA OG2 RED LF W/TAG 2. CA OG2 GR ROMN W/TG 3. USA/MEX OG2 BUTTER LETTCE 4. USA OG2 LIVING BUTTER
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2093-2025·2025-07-16

    TrueDent Yellow dental resin cartridges carry an expiration date formatting error

    TrueDent Yellow dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 68 units are affected.

    Product
    TrueDent Yellow, TDM140, Model No. OBJ-09169 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2107-2025·2025-07-16

    Preat Astra dental analogs have rotational feature 180 degrees off

    Preat Astra EV-compatible 4.2 mm Digital Analogs are being recalled because a manufacturing error left the digital analog rotational feature 180 degrees off. 44 units are affected.

    Product
    Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0512-2025·2025-07-16

    B Natural Organics mineral sunscreens recalled over manufacturing practice deviations

    B Natural Organics Organic Sunscreen SPF 30, in tinted and tint free formulas, is being recalled because of cGMP deviations. 204 tubes are affected.

    Product
    B Natural Organics, Organic Sunscreen, Broad Spectrum, SPF 30, 25% non-nano Zinc Oxide, a) Nude Tint Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1002-2; b) Tint Free Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1001-2; c)
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Food)·H-0232-2025·2025-07-16

    Organic broccoli bunches and crowns recalled over reach truck fluid contamination

    Organic broccoli bunches, wrapped broccoli and broccoli crowns are being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.

    Product
    1. BROCCOLI OG2 BROCCOLI BUNCH 2. WLD HRVST OG2 BROCCOLI WRPP 3. USA OG2 BROCCLI CRWNS
    Category
    Food
    Distribution
    5 states