The Recall Desk

State

New York product recalls

73,213 recalls have nationwide distribution and so reach New York. 12,939 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,939
Critical
1,511
Severe
3,148
Most recent
2026-09-30

Of the 12,939 recalls naming New York we have scored against our rubric, 1,511 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,148 (24%) are Severe.

These figures cover only the 12,939 recalls whose distribution notice names New York specifically. The 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15176–15200 of 86152

  • HighFDA (Devices)·Z-0414-2024·2023-12-06

    Edwards TruWave pressure monitoring kit recalled for setup issues

    Edwards Lifesciences is recalling 168,014 TruWave with Vamp pressure monitoring kits due to potential flushing difficulties during setup. The recall affects devices distributed across the US and internationally.

    Product
    TruWave with Vamp System Pressure monitoring set, REF: PXAVMP(3cc)/VAMP 68 in (173cm) PXAVMP3: x3 (3cc)/VAMP PXVK0364:(3cc)/VAMP 96in (241cm); PXVK0853: x3 (3cc)/VAMP 76in (193cm); PXVK0996:(3cc)/VAMP 68in (174cm); PXVMP2X21: x2 (3cc)/VAMP; PXVMP2X22: x2 (3cc)/VAMP 63 in…
    Category
    Medical Device
    Distribution
    51 states
  • HighFDA (Devices)·Z-0406-2024·2023-12-06

    Da Vinci Needle Driver Recalled for Risk of Dislodgement During Surgery

    Intuitive Surgical is recalling 317 units of a Da Vinci Single-Site Wristed Needle Driver due to potential dislodgement or breakage that could result in uncontrollable movement.

    Product
    Da Vinci Single-Site Wristed Needle Driver, REF: 478115, 5 mm
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Food)·F-0470-2024·2023-12-06

    Frito-Lay Chickpea Veggie Crisps recalled for undeclared milk allergen

    Frito-Lay is recalling 16,100 bags of Chickpea Veggie Crisps (UPC 02840020646) due to undeclared milk allergen. Consumers with milk allergies should not consume the product.

    Product
    Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-0419-2024·2023-12-06

    Olympus EVIS EXERA III Colonoscope Recall for Connector Defect

    24 Olympus EVIS EXERA III colonoscopes distributed to six states are recalled due to improperly repaired connectors that may cause image loss, decreased suction, or improper reprocessing, potentially exposing patients to contaminated equipment.

    Product
    PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0423-2024·2023-12-06

    RAPIDPOINT 500 Blood Gas System: Drug Interference May Cause False Sodium Readings

    Siemens RAPIDPOINT 500 Blood Gas System may produce falsely elevated sodium results due to drug interference from Perhexiline Maleate or Atomoxetine Hydrochloride. This could lead to missed hyponatremia or inappropriate treatment of hypernatremia.

    Product
    RAPIDPOINT 500 Blood Gas System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0422-2024·2023-12-06

    RAPIDPOINT 500e Blood Gas System Recalled Due to Drug Interference

    Siemens RAPIDPOINT 500e blood gas systems may show falsely elevated sodium readings in patients taking Perhexiline Maleate or Atomoxetine, risking misdiagnosis and inappropriate treatment of electrolyte imbalances.

    Product
    RAPIDPOINT 500e Blood Gas System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0411-2024·2023-12-06

    FloTrac Sensor Recalled Due to Potential Flushing Difficulties During Setup

    Edwards Lifesciences is recalling 1417 FloTrac Sensors used for intravascular pressure monitoring due to potential flushing difficulties during kit setup. No illnesses or injuries have been reported.

    Product
    FloTrac Sensor, REF: MHD8 & MHD85,MHD6R5, MHD8R, MHD8R5, MHD8S, STERILEEO, Rx only. For use in intravascular pressure monitoring.
    Category
    Medical Device
    Distribution
    51 states
  • HighFDA (Devices)·Z-0409-2024·2023-12-06

    Acumen IQ Sensor Intravascular Pressure Monitor Flushing Difficulty

    Edwards Lifesciences is recalling 33,327 Acumen IQ Sensors used for intravascular pressure monitoring due to potential flushing difficulties during setup. The devices are distributed across the US and internationally.

    Product
    Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in intravascular pressure monitoring.
    Category
    Medical Device
    Distribution
    51 states
  • HighFDA (Devices)·Z-0418-2024·2023-12-06

    Colonoscope Repair Defect May Cause Device Malfunction and Contamination Risk

    Aizu Olympus colonoscopes with improperly repaired light guide connectors may experience loss of image or suction failure. This could delay treatment and expose patients to contaminated material.

    Product
    PCF-H190DL, EVIS EXERA III COLONOVIDEOSCOPE
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-0130-2024·2023-12-06

    Paroxetine 40 mg tablets recalled for out-of-specification impurities

    Golden State Medical Supply Inc. is recalling Paroxetine 40 mg tablets due to failed impurity specifications. A total of 5,626 bottles were distributed nationwide.

    Product
    PAROXETINE — PAROXETINE (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0125-2024·2023-12-06

    Compounded Ophthalmic Medication Bottles Mislabeled as Single-Use Syringes

    Fagron Compounding Services is recalling 756 bottles of compounded ophthalmic medication because labels incorrectly identify the container as a 0.5mL single-use syringe instead of a 5mL dropper bottle. No adverse events have been reported.

    Product
    Tropicamide 1% (10mg/mL), Cyclopentolate 1% (10mg/mL), Phenylephrine 2.5% (25mg/mL), Ketorolac 0.5% (5mg/mL), 5 mL bottles, For Topical Ophthalmic Use Only, Not for IV Use, This is a Compounded Drug, Hospital & Office Use Only, Fagron Sterile Services, 8710 E 34th St N Wichita…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0129-2024·2023-12-06

    Paroxetine 20 mg Tablets Recalled for Out-of-Specification Impurity

    Golden State Medical Supply is recalling certain lots of Paroxetine 20 mg tablets nationwide due to an out-of-specification chemical impurity in the product.

    Product
    PAROXETINE — PAROXETINE (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0410-2024·2023-12-06

    Intravascular Pressure Sensor Recalled for Flushing Difficulties During Setup

    Edwards Lifesciences is recalling Acumen IQ intravascular pressure monitoring sensors (6,714 units) due to potential flushing difficulties during setup of the pressure monitoring kit.

    Product
    Acumen IQ Sensor with VAMP System, REFs: AIQS6AZ & AIQS6AZ5, STERILEEO, Rx only. For use in intravascular pressure monitoring.
    Category
    Medical Device
    Distribution
    51 states
  • ModerateFDA (Drugs)·D-0127-2024·2023-12-06

    Testosterone Gel Recalled for Out-of-Specification Viscosity

    Teva Pharmaceuticals recalls specific lots of Testosterone Gel 1.62% for failing viscosity specifications. Patients should contact their healthcare provider to discuss the recall and obtain unaffected medication.

    Product
    TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0413-2024·2023-12-06

    TruWave Pressure Monitoring Set Recalled for Potential Flushing Difficulties

    Edwards Lifesciences is recalling 118,570 units of the TruWave Pressure Monitoring Set due to potential flushing difficulties during setup. The device is used for hemodynamic pressure monitoring.

    Product
    TruWave Pressure monitoring set, REF: PX212: cc/12 in (30cm), PX260: (3 cc/60in (150cm), PX272: 3 cc/72in (180cm), PX284: 3 cc/84 in (210 cm), PX2X2: x2 (3cc), PX3X3284C: X3 (3cc), PX4X4: x4 (3cc), PX600F (3cc), PXMK1876: x 3 (3 cc), PXMK1940: (3 cc), PXMK2024: (3cc)/77 in…
    Category
    Medical Device
    Distribution
    51 states
  • ModerateFDA (Drugs)·D-0126-2024·2023-12-06

    VistaPharm Recalls Aminocaproic Acid Oral Solution Due to High Ethylene Glycol

    VistaPharm LLC is recalling Aminocaproic Acid Oral Solution (0.25 grams/mL) distributed nationwide due to high ethylene glycol content from failed manufacturing specifications. Four lot numbers are affected.

    Product
    Aminocaproic Acid Oral Solution, 0.25 grams/mL, Rx only, packaged in 8 Fl. Oz. (236.5 mL) HDPE bottles, Manufactured for: VistaPharm, Inc., Largo, FL 33771, UAS, NDC 66689-330-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0412-2024·2023-12-06

    FloTrac Pressure Monitoring Sensor Recalled for Setup Flushing Difficulties

    Edwards Lifesciences' FloTrac Sensor with Vamp System is being recalled due to potential flushing difficulties during setup of the pressure monitoring kit. No injuries have been reported.

    Product
    FloTrac Sensor with Vamp System, REF: MHD6AZ, MHD6AZ5 , MHD6C502 STIRLEEO, Rx only. For use in intravascular pressure monitoring.
    Category
    Medical Device
    Distribution
    51 states
  • ModerateFDA (Drugs)·D-0120-2024·2023-12-06

    Paroxetine Tablets Recalled Due to Manufacturing Specification Failure

    Apotex Corp. is recalling Paroxetine Hydrochloride 20 mg tablets nationwide due to out-of-specification impurity levels in affected lots. No illnesses have been reported.

    Product
    PAROXETINE — PAROXETINE (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V815000·2023-12-05

    Terberg Benschop Recalls Terminal Tractors for Steering Linkage Defect

    Terberg Benschop is recalling 2021-2022 YT193 terminal tractors because paint wear on the steering linkage may cause bolts to loosen or break, risking loss of steering control.

    Product
    TERBERG BENSCHOP B.V. — TERBERG BENSCHOP B.V. TERMINAL TRACTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V817000·2023-12-05

    Cushman Recalls 2024 Hauler Pro LSVs Due to Fire Risk

    Textron Specialized Vehicles is recalling 2024 Cushman Hauler Pro LSVs because water may enter the battery module, damaging circuits and increasing fire risk.

    Product
    CUSHMAN — CUSHMAN HAULER PRO LSV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24726·2023-12-05

    Foiresoft Zebra Roller Blinds Recalled for Strangulation Hazard

    Foiresoft Zebra Roller Blinds sold on Amazon.com have looped operating cords that pose a strangulation hazard to children. Consumers should stop using them immediately and contact Softfunch for a refund.

    Product
    Foiresoft Zebra Roller Blinds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V816000·2023-12-05

    Volvo 2024 VN and VHD: Incorrect Axle Weight Label Increases Overload Risk

    Certain 2024 Volvo VN and VHD trucks have an incorrect Gross Axle Weight Rating label, which can allow vehicles to be overloaded and increases crash risk. Dealers will replace the label free of charge.

    Product
    VOLVO — VOLVO VN, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V811000·2023-12-04

    Eldorado Axess and EZR Buses Recalled for Driveshaft Separation Risk

    Eldorado is recalling 2019-2023 Axess and EZR buses because a transmission yoke may separate, causing a sudden loss of drive power and increasing crash risk.

    Product
    ELDORADO — ELDORADO AXESS, EZR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V812000·2023-12-04

    Gillig Recalls 2021-2023 Low Floor Vehicles Due to Fire Risk

    Gillig is recalling 3,626 Low Floor vehicles from 2021-2023 because an incorrect fuse in the rearview mirror system may overheat and cause a fire.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V813000·2023-12-04

    Porsche Recalls 718 Models Due to Spoiler Visibility Issue

    Porsche is recalling certain 2023-2024 718 models because the rear spoiler may raise too high, reducing brake light visibility and increasing crash risk.

    Product
    PORSCHE — PORSCHE 718 BOXSTER S, 718 CAYMAN GTS, 718 BOXSTER GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide