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.

Which agencies issued them

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.

42176–42200 of 86765

  • ModerateFDA (Devices)·Z-0651-2019·2018-12-26

    Ortho-Clinical Diagnostics Recalls VITROS 5,1 FS Chemistry System Software

    Ortho-Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry Systems due to a software anomaly that may incorrectly extend reagent stability time.

    Product
    VITROS 5,1 FS Chemistry System, Version 3.0 & below For use in the in vitro quantitative measurement of a variety of analytes of clinical interest in certain biological fluids (depending on the analyte) such as serum, plasma, urine and cerebrospinal fluid.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0630-2019·2018-12-26

    Zimmer Biomet Recalls NexGen Knee Augment Blocks Due to Missing Screws

    Zimmer Biomet is recalling 19 NexGen Complete Knee Solution Femoral Augment Blocks because a screw is missing from the package.

    Product
    NexGen¿ Complete Knee Solution Femoral Augment Block Distal only, 15mm, Size E with Screw Item Number: 00599003523 NexGen Distal Femoral Augment Block is used when femoral components can neither be downsized nor can be distally augmented by increasing the thickness of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0613-2019·2018-12-26

    Tosoh AIA-360 Analyzer Recalled for Table Home Sensor Malfunction

    Tosoh Bioscience Inc is recalling 438 AIA-360 Analyzers because a table home sensor malfunction can cause the device to stop functioning, potentially delaying patient test results.

    Product
    AIA-360 Analyzer is capable of performing two methods of immunoassay: an immunoenzymetric (IEMA) or sandwich immunoassay, a competitive binding (EIA) immunoassay. An antigen-antibody reaction begins by combining a patient sample, control, or calibrator with a diluent in an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0382-2019·2018-12-26

    Cipla Recalls Nevirapine Extended Release Tablets for Dissolution Failure

    Cipla Limited is recalling 4,800 bottles of Nevirapine Extended Release Tablets, 400 mg, because they failed to meet dissolution specifications.

    Product
    Nevirapine Extended Release Tablets, 400 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd. Verna Goa, India, Manufactured for: Cipla USA Inc. 9100 S Dadeland Blvd., Suite 1500 Miami, FL 33156, NDC 69097-403-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0637-2019·2018-12-26

    Cardinal Health Recalls Protexis Neoprene Surgical Gloves Due to Labeling Error

    Cardinal Health is recalling Protexis Neoprene Surgical Gloves because the packaging contains incorrect breakthrough times for specific chemotherapy drugs.

    Product
    Protexis Neoprene Surgical Glove, Size 8.5 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0638-2019·2018-12-26

    Cardinal Health Recalls Protexis Neoprene Surgical Gloves Due to Labeling Errors

    Cardinal Health is recalling Protexis Neoprene Surgical Gloves because the primary packaging contains incorrect breakthrough times for specific chemotherapy drugs.

    Product
    Protexis Neoprene Surgical Glove, Size 9.0 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0611-2019·2018-12-26

    Diagnostica Stago Recalls Staclot LA 20 Test Kits Due to Result Variability

    Diagnostica Stago is recalling Staclot LA 20 test kits because some results showed shortened times outside the expected range.

    Product
    Staclot LA 20 (REF 00594) The Staclot¿ LA and Staclot¿ LA 20 test kits are reagent systems designed for the qualitative detection of lupus anticoagulants (LA) in plasma by the use of hexagonal HII phase phospholipid molecules (1, 2).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0640-2019·2018-12-26

    Advanced Instruments Recalls GloCyte RBC Reagent Due to QC Failure

    Advanced Instruments, LLC is recalling GloCyte RBC Reagent because high fluorescent counts cause quality control checks to fail, preventing patient sample testing.

    Product
    GloCyte RBC Reagent - Product Usage: The GloCyte Automated Cell Counter System is intended for use by trained healthcare professionals in clinical laboratories to provide quantitative determination of fluorescence labeled total nucleated cells and erythrocytes in cerebrospinal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0634-2019·2018-12-26

    Cardinal Health Recalls Protexis Neoprene Surgical Gloves Due to Labeling Errors

    Cardinal Health 200, LLC is recalling Protexis Neoprene Surgical Gloves because the primary packaging contains incorrect breakthrough times for specific chemotherapy drugs.

    Product
    Protexis Neoprene Surgical Glove, Size 7.0 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0633-2019·2018-12-26

    Cardinal Health Recalls Protexis Neoprene Surgical Gloves Due to Labeling Errors

    Cardinal Health is recalling Protexis Neoprene Surgical Gloves because the packaging lists incorrect breakthrough times for specific chemotherapy drugs.

    Product
    Protexis Neoprene Surgical Glove, Size 6.5 This powder-free Surgeon s glovessterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0656-2019·2018-12-26

    COVIDIEN Recalls 8Fr Argyle Suction Catheter Kits with Chimney Valve

    COVIDIEN LLC is recalling 32,071 units of 8Fr Argyle Suction Catheter Kits with Chimney Valve, Model 36826, because they were distributed while subject to importation refusal.

    Product
    8Fr SAFE GRAD CAT W/Valve (Argyle Suction Catheter Kits with Chimney Valve), Model Number 36826
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-0632-2019·2018-12-26

    Cardinal Health Recalls Protexis Neoprene Surgical Gloves Due to Labeling Error

    Cardinal Health 200, LLC is recalling Protexis Neoprene Surgical Gloves because the primary packaging contains incorrect breakthrough times for specific chemotherapy drugs.

    Product
    Protexis Neoprene Surgical Glove, Size 6.0 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0635-2019·2018-12-26

    Cardinal Health Recalls Protexis Neoprene Surgical Gloves Due to Labeling Error

    Cardinal Health 200, LLC is recalling Protexis Neoprene Surgical Gloves because the packaging contains incorrect breakthrough times for specific chemotherapy drugs.

    Product
    Protexis Neoprene Surgical Glove, Size 7.5 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0653-2019·2018-12-26

    Ortho-Clinical Diagnostics Recalls VITROS 4600 Chemistry System Software

    Ortho-Clinical Diagnostics is recalling 728 VITROS 4600 Chemistry Systems because a software anomaly may incorrectly extend reagent stability time.

    Product
    VITROS 4600 Chemistry System, Version 3.3.1 & below For use in the in vitro quantitative measurement of a variety of analytes of clinical interest in certain biological fluids (depending on the analyte) such as serum, plasma, urine and cerebrospinal fluid.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0631-2019·2018-12-26

    Cardinal Health Recalls Protexis Neoprene Surgical Gloves Due to Labeling Error

    Cardinal Health 200, LLC is recalling Protexis Neoprene Surgical Gloves because the primary packaging contains incorrect breakthrough times for specific chemotherapy drugs.

    Product
    Protexis Neoprene Surgical Glove, Size 5.5 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0642-2019·2018-12-26

    Zimmer Biomet Compress System Surgical Technique Correction Recall

    Zimmer Biomet is correcting the surgical technique for the Compress System to update selection criteria for anti-rotation pin placement.

    Product
    Zimmer Compress Devices and Instruments: Item Number/Item Description 178350 Compress Device Anti-Rotation Spindle 178353 Compress Device Anti-Rotation Spindle 178356 Compress Device Anti-Rotation Spindle 178359 Compress Device Anti-Rotation Elliptical Spindle 178537…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0348-2019·2018-12-26

    VistaPharm Recalls Nystatin Oral Suspension Due to Impurity Failures

    VistaPharm is recalling Nystatin Oral Suspension because it failed impurity specifications. The affected product is distributed nationwide and in Puerto Rico.

    Product
    NYSTATIN Oral Suspension, USP 500,000 Units/5mL, unit dose 5ml cups, packaged in a) 50 unit dose cups (10x5ml unit dose cups per tray, 5 trays per case) NDC 66689-037-50; b) 100 unit dose cups (10x5ml unit dose cups per tray, 10 trays per case) NDC 66689-037-99. Rx Only…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V928000·2018-12-21

    Prevost Recalls Buses Due to Draglink Fracture Risk

    Prevost is recalling 676 buses because a steering component may fracture, causing a loss of steering and increasing crash risk.

    Product
    PREVOST — PREVOST X3-45, XLII-45, XL-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V930000·2018-12-21

    Thomas Built Saf-T-Liner C2 School Bus Recall for Electrical Overload

    Daimler Trucks is recalling 2019-2020 Thomas Built Saf-T-Liner C2 school buses because an electrical overload may cause the engine to shut down, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V924000·2018-12-21

    Collins Recalls 2018 Buses Due to Improperly Tightened Seat Bolts

    Collins Bus Corporation is recalling 2018 SH, DH, P24, T22, T24, and TH buses because seat bolts may not be properly tightened, increasing injury risk in a crash.

    Product
    COLLINS — COLLINS T24, DH, TH, T22
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·124-2018·2018-12-21

    Jennie-O Recalls Raw Ground Turkey Due to Salmonella Reading Contamination

    Jennie-O is recalling approximately 164,210 pounds of raw ground turkey products produced in October 2018 due to possible Salmonella Reading contamination.

    Product
    Jennie-O Turkey Store — Jennie-O Turkey Store Sales, Inc. Recalls Raw Ground Turkey Products due to Possible Salmonella Reading Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V929000·2018-12-21

    Thomas Built Buses Recalls Saf-T-Liner C2 for Electrical Overload Risk

    Daimler Trucks North America is recalling 2019-2020 Thomas Built Saf-T-Liner C2 buses because an electrical overload may cause the engine to shut down, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V927000·2018-12-21

    Harley-Davidson Recalls Street Motorcycles Due to Brake Caliper Corrosion

    Harley-Davidson is recalling 2016-2019 Street 500, 750, and 750A motorcycles because brake calipers may corrode internally, causing increased brake drag and a higher risk of crash.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON XG500, XG750A, XG750
    Category
    Vehicle
    Distribution
    Distributed nationwide