The Recall Desk

State

New York product recalls

73,741 recalls have nationwide distribution and so reach New York. 12,955 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,955
Critical
1,508
Severe
3,701
Most recent
2026-10-28

Of the 12,955 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 3,701 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,955 recalls whose distribution notice names New York specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37476–37500 of 86696

  • ModerateFDA (Devices)·Z-2556-2019·2019-10-02

    Arrow Central Venous Catheterization Kit Recalled for Incorrect Banner Card

    Arrow International Inc is recalling 231 units of 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kits because they may contain the incorrect banner card.

    Product
    Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2551-2019·2019-10-02

    Sentinel CH SpA Recalls MULTIGENT Lithium Reagent Kits

    Sentinel CH SpA is recalling 15,919 MULTIGENT Lithium reagent kits due to a potential carryover issue that may cause falsely elevated patient results.

    Product
    MULTIGENT Lithium-intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 8L25-30
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1882-2019·2019-10-02

    FDA Recalls Oxaliplatin Active Pharmaceutical Ingredient Due to Glass Contamination

    Johnson Matthey Inc. is recalling Oxaliplatin Active Pharmaceutical Ingredient due to potential glass contamination. The product was distributed nationwide in the United States.

    Product
    Oxaliplatin Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West Deptford, NJ 08066-1742 (856) 384-7001, NDC 49821-0075-XX
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2755-2019·2019-10-02

    Abbott APS Accelerator Modules Recalled for Missing Pacemaker Safety Label

    Abbott is recalling 159 APS Accelerator modular systems because the safety pacemaker label is missing. The Operations Manual has been updated to specify a 200 mm minimum safety distance for pacemaker wearers.

    Product
    APS Accelerator modular systems, 208-230 V-, 50/60 Hz, 1800 VA, IVD, RX, Class 2 Laser Product,
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-2553-2019·2019-10-02

    GN Otometrics Recalls Gold Cup and Snap Leadwires Due to Conductor Defect

    GN Otometrics is recalling Gold Cup and Snap Leadwires because the electrode lead connector has a protruding conductor beyond the insulation.

    Product
    Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap Leadwire, Blue; 3. 24" Snap Leadwire, Red; 4. 40" Snap Leadwire, Red; 5. 24" Snap Leadwire, Green; 6. 40" Snap Leadwire, Green…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2554-2019·2019-10-02

    Smiths Medical Medfusion 4000 Syringe Infusion Pump Recall for Wireless Connectivity Issues

    Smiths Medical is recalling Medfusion 4000 Syringe Infusion Pumps with PharmGuard Server Software due to potential wireless network connectivity issues caused by a Radio Module defect.

    Product
    Medfusion¿ Model 4000 Syringe Infusion Pump, with PharmGuard¿ Server Software (PGS). Sold under the following names: MEDFUSION¿ 4000 Pump V1.0; MEDFUSION¿ 4000 Pump V1.1, v1.1.1, v1.1.2; MEDFUSION¿ 4000 Pump V1.1, V1.1.1, V1.1.2; MEDFUSION¿ 4000 Pump V1.5, V1.5.1…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1880-2019·2019-10-02

    Fentanyl Citrate Ingredient Recalled for Potential Glass Contamination

    Johnson Matthey Inc. is recalling fentanyl citrate active pharmaceutical ingredient due to potential glass contamination.

    Product
    Fentanyl Citrate Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West Deptford, NJ 08066-1742 (856) 384-7001.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2558-2019·2019-10-02

    V-Twin Automated Chemistry Analyzer Recalled for Software Lockup

    Vital Scientific N.V. is recalling two V-Twin automated chemistry analyzers in New York because a software lockup prevents the instruments from producing patient results.

    Product
    V-Twin, Model # 6002-800, UDI: 03661540600180 Product Usage: An in-vitro diagnostic device, which is an automated chemistry analyzer, micro type, intended for clinical use in conjunction with certain materials to measure a variety of analytes, including applications in…
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2754-2019·2019-10-02

    Siemens Recalls Atellica IM Anti-CCP IgG Assay Due to Mitigation Failure

    Siemens Healthcare Diagnostics is recalling 169 kits of the Atellica IM anti-CCP IgG assay because a reagent carryover mitigation step fails to complete on the analyzer.

    Product
    Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998 (100 Test) Test Version1.0 - Product Usage: The ADVIA Centaur¿ Anti-CCP IgG (aCCP) assay is for in vitro diagnostic use in the semi-quantitative determination of the IgG class of autoantibodies specific to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2753-2019·2019-10-02

    Accu-Chek Connect App Recall for Android Data Transfer Failure

    Roche Diabetes Care is recalling the Accu-Chek Connect App because users on Android OS 8.0 and above may be unable to transfer meter values to the app.

    Product
    Accu-Chek Connect Diabetes Management App
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2250-2019·2019-10-02

    Udi's Classic Hamburger Buns Recalled for Potential Foreign Material

    ConAgra Foods is recalling Udi's Classic Hamburger Buns due to the potential presence of foreign material. The product was distributed to wholesale and retail locations in 13 states.

    Product
    Udi's Classic Hamburger Buns, packaged in a 10.4 oz. plastic bag, with eight bags per wholesale case. UPC 00-6-98997-80913-5 .
    Category
    Food
    Distribution
    13 states
  • ModerateFDA (Drugs)·D-1878-2019·2019-10-02

    Akorn Recalls Lidocaine Hydrochloride Jelly Due to Metal Particulate Finding

    Akorn, Inc. is recalling Lidocaine Hydrochloride Jelly USP, 2% due to a finding of metal particulate matter in the filling room. No particulates were identified in the product itself.

    Product
    Lidocaine Hydroclhoride Jelly USP, 2%, 30 mL tubes, Rx Only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-711-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2555-2019·2019-10-02

    Arrow International Recalls Central Venous Access Kits Due to Incorrect Banner Card

    Arrow International Inc is recalling 520 units of ARROW+gard Blue PSI Kit Cath-Gard central venous access devices because they may contain the incorrect banner card.

    Product
    8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard for use with 7.5 - 8 Fr.Catheters Product Code: CDC-29803-1A - Product Usage: The MACTM Two-Lumen Central Venous Access Device with ARROWg+ard Blue¿ permits venous access and catheter introduction to the central circulation. It…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0001-2020·2019-10-02

    Pfizer Recalls Ethosuximide Capsules Due to Incorrect Expiration Date Labeling

    Pfizer is recalling 7,824 bottles of ethosuximide capsules because the expiration date on the label is incorrect.

    Product
    ethosuximide capsules, USP, 250 mg, 100-count bottle, Rx Only, Distributed by: Greenstone LLC Peapack, NJ 07977 Made in Netherlands. NDC 59762-2250-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2557-2019·2019-10-02

    Randox Urinalysis Control Level 2 Recalled for Incorrect Leukocyte Range

    Randox Laboratories is recalling Randox Urinalysis Control Level 2 kits because the leukocyte range for the Siemens Multistix method was incorrect.

    Product
    Randox Urinalysis Control Level 2 (IVD) Ref: UC5034 - Product Usage: Product is intended for in vitro diagnostic use in the quality control of urine test strips.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V692000·2019-10-01

    BMW Recalls 2017-2020 K 1600 Series Motorcycles for Transmission Defect

    BMW is recalling 2017-2020 K 1600 GT, GTL, and B motorcycles because transmission parts may not be hard enough, risking rear wheel lockup and crashes.

    Product
    BMW — BMW K1600B, K 1600 GTL, K 1600 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V690000·2019-10-01

    Jayco Recalls 2019-2020 Redhawk SE Motorhomes for Seatbelt Warning Defect

    Jayco is recalling 2019-2020 Redhawk SE motorhomes because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition, increasing crash injury risk.

    Product
    JAYCO — JAYCO REDHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V688000·2019-09-30

    Ford Recalls 2019 F-250 and F-350 Trucks for Rear Axle Defect

    Ford is recalling 28,579 2019 F-250 and F-350 trucks because the passenger-side rear axle shaft may fail prematurely, potentially causing loss of drive power or unintended movement.

    Product
    FORD — FORD redundant F-250, redundant F-350
    Category
    Vehicle
    Distribution
    Distributed nationwide