The Recall Desk

State

New York product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31901–31925 of 86692

  • HighFDA (Devices)·Z-0066-2021·2020-10-14

    Medline Recalls Non-Sterile Cath Lab Kits Sold Without Sterilization Capability

    Medline Industries is recalling 32 non-sterile cath lab kits because they were sold to accounts without the capability to sterilize them prior to use.

    Product
    Kit Model #650600111, MTO Left Heart St Francis Hosp - PG - Product Usage: NAMIC Cath Lab and Interventional Radiology (IR) Kits consist of any combination of devices from the NAMIC Fluid Management finished good product families and potentially other devices designed and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0073-2021·2020-10-14

    Biomet 3i Recalls Misaligned BellaTek Encode Definitive Abutments

    Biomet 3i, LLC is recalling BellaTek Encode Definitive Abutments because the hex was misaligned by 30 degrees during manufacturing, preventing correct placement in patients.

    Product
    BellaTek Encode Defin3DPMSERitive Abutments-3D Printed Model Reference Numbers: 3DPMSER, 3DPMSERQ
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0069-2021·2020-10-14

    Nuvasive Precice Bone Transport System Recall for Distal Plug Disassociation Risk

    Nuvasive is recalling 41 Precice Bone Transport System units because standard removal tools can cause the distal plug to disassociate during explantation.

    Product
    NUVASIVE SPECIALIZED ORTHOPEDICS, INC. Precice Bone Transport Antegrade Femur Trochanter 10 Degree Bend Component of the orthopedic Precice Bone Transport System of intramedullary nail, locking screws, reusable instruments, and hand-held External Remote Controller (ERC).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0065-2021·2020-10-14

    Medline Recalls Non-Sterile Cath Lab Kits Sold Without Sterilization Capability

    Medline Industries is recalling 16 non-sterile cath lab kits that were sold to accounts without the ability to sterilize them prior to use.

    Product
    Kit Model #650305414, MTO Left Heart with DT Boulder Com Hosp - Product Usage: NAMIC Cath Lab and Interventional Radiology (IR) Kits consist of any combination of devices from the NAMIC Fluid Management finished good product families and potentially other devices designed and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0050-2021·2020-10-14

    Ra Medical Systems Recalls DABRA RA-308 Excimer Laser Units

    Ra Medical Systems is recalling 54 DABRA RA-308 Excimer Laser units because a taller wheel mounting may cause the device to fall over, potentially injuring users or patients.

    Product
    DABRA RA-308 Excimer Laser, SN: ******* - Product Usage: The device is intended for use in ablating a channel in occlusive peripheral vascular disease.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0080-2021·2020-10-14

    Bard Conquest PTA Balloon Catheter Recalled for Incorrect Balloon Size

    Bard Peripheral Vascular Inc is recalling 281 units of the Conquest PTA Balloon Dilation Catheter because some units contain a 5mm balloon instead of the labeled 6mm size.

    Product
    Bard Conquest PTA Balloon dilation Catheter, 6mm x 40mm, 75 cm, Cat. No. CQ7564, UDI: (01) 00801741062902 - Product Usage: use in Percutaneous Transluminal Angioplasty of the femoral, iliac, and renal arteries and for the treatment of obstructive lesions of native or synthetic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0077-2021·2020-10-14

    Biomet 3i Recalls BellaTek Titanium Abutments Due to Manufacturing Misalignment

    Biomet 3i is recalling 35 units of BellaTek Titanium Abutments because the hex was misaligned by 30 degrees during manufacturing, preventing correct placement.

    Product
    CERTAIN BELLATEK TITANIUM ABUTMENT 4.1MM Reference Number: IEDAT4
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Food)·F-0013-2021·2020-10-14

    Nettle Meadow Artisan Cheese Recalled Due to Unrecorded Pasteurization Temperature

    LuMaZu, LLC dba Nettle Meadow is recalling two cases of Habanero Peach Fromage Frais because pasteurization temperatures were not recorded due to a recorder malfunction.

    Product
    "Nettle Meadow Artisan Cheese *** Habanero Peach Fromage Frais***Contains pasteurized goat and cows milk*** 5 oz."
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0010-2021·2020-10-14

    Nettle Meadow Apple Cider Fromage Frais Recalled Due to Pasteurization Record Failure

    LuMaZu, LLC dba Nettle Meadow is recalling 5 oz. Apple Cider Fromage Frais because pasteurization temperatures were not recorded for two lots due to a recorder malfunction.

    Product
    "Nettle Meadow Artisan Cheese ***Apple Cider Fromage Frais*** Contains pasteurized goat and cows milk*** 5 oz."
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0074-2021·2020-10-14

    Biomet 3i Recalls Misaligned BellaTek Titanium Abutments

    Biomet 3i is recalling BellaTek Titanium Abutments because the hex was misaligned by 30 degrees during manufacturing, preventing correct placement in patients.

    Product
    BELLATEK TITANIUM ABUTMENT 4.1MM Reference Number: EDAT4
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0053-2021·2020-10-14

    Ultradent PermaFlo Flowable Composite Recalled for Manufacturing Cross-Contamination

    Ultradent Products, Inc. is recalling PermaFlo Flowable Composite due to a potential manufacturing issue causing cross-contamination and non-homogeneity.

    Product
    PermaFlo Flowable Composite REF-UP 948 Shade: A2 - Product Usage: is a light cured, radiopaque, methacrylate based, flowable composite. PermaFlo contains H1¿m average particle size with narrow upper limit particle distribution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0009-2021·2020-10-14

    Nettle Meadow Fig Honey Fromage Frais Recalled for Pasteurization Record Failure

    LuMaZu, LLC dba Nettle Meadow is recalling Fig Honey Fromage Frais because pasteurization temperatures were not recorded for two lots due to a recorder malfunction.

    Product
    "Nettle Meadow Artisan Cheese *** Fig Honey Fromage Frais*** Contains pasteurized goat and cows milk*** 5 oz.***"
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0012-2021·2020-10-14

    Nettle Meadow Truffle Fromage Frais Recalled Due to Pasteurization Record Failure

    LuMaZu, LLC dba Nettle Meadow is recalling 16 units of Truffle Fromage Frais because pasteurization temperatures were not recorded for two lots due to a recorder malfunction.

    Product
    "Nettle Meadow Artisan Cheese *** Truffle Fromage Frais***Contains pasteurized goat and cows milk*** 5 oz."
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0076-2021·2020-10-14

    Biomet 3i Recalls BellaTek Abutments Due to Manufacturing Misalignment

    Biomet 3i is recalling 4 units of BellaTek abutments because the hex was misaligned by 30 degrees, preventing correct placement in patients.

    Product
    CERTAIN BELLATEK TIN ABUTMENT 5.0MM Reference Number: IEDAN5
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0056-2021·2020-10-14

    Brainlab Ultrasound Navigation Software Recalled for Image Width Limitation

    Brainlab AG is recalling Ultrasound Navigation Software 1.0 and related integration software because the system does not support modifying the probe's image width.

    Product
    Ultrasound Navigation Software 1.0 and Ultrasound Integration Software for Cranial/ENT Navigation 3.0.x and 3.1.x - Product Usage: intended to be an intra-operative image guided localization system to enable minimally invasive surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0052-2021·2020-10-14

    Siemens Troponin I Reagent Cartridge Recalled for Positive Bias

    Siemens Healthcare Diagnostics is recalling Dimension LOCI High Sensitivity Troponin I reagent cartridges due to positive bias in test results.

    Product
    Dimension LOCI High Sensitivity Troponin I (TNIH) Flex reagent cartridge-IVD-In vitro diagnostic use in the quantitative measurement of cardiac troponin I in human plasma Catalog Number: RF627, SMN# 10471068
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0030-2021·2020-10-14

    Skippy Super Chunk Peanut Butter Recalled for Aflatoxin Levels

    Hormel Foods is recalling Skippy Super Chunk Peanut Butter because aflatoxin levels were slightly above the actionable limit.

    Product
    SKIPPY Super Chunk Peanut Butter 16.3oz UPC: 00037600110723 packaged in non-flexible plastic container
    Category
    Food
    Distribution
    35 states
  • ModerateFDA (Devices)·Z-0075-2021·2020-10-14

    Biomet 3i Recalls Misaligned BellaTek Dental Abutments

    Biomet 3i is recalling 9 units of BellaTek Encode Definitive Abutments because the hex was misaligned by 30 degrees during manufacturing, preventing correct placement.

    Product
    CERTAIN BELLATEK TIN ABUTMENT 4.1MM Reference Number: IEDAN4
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Food)·F-0011-2021·2020-10-14

    Nettle Meadow Artisan Cheese Recalled Due to Pasteurization Recording Failure

    LuMaZu, LLC dba Nettle Meadow is recalling artisan cheese because pasteurization temperatures were not recorded for two lots due to a recorder malfunction.

    Product
    "Nettle Meadow Artisan Cheese *** Roasted Red Pepper Fromage Frais***Contains pasteurized goat and cows milk***5 oz."
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0078-2021·2020-10-14

    Biomet 3i Recalls BellaTek Titanium Abutments Due to Manufacturing Misalignment

    Biomet 3i is recalling 10 units of BellaTek Titanium Abutments because the hex was misaligned by 30 degrees during manufacturing, preventing correct placement.

    Product
    CERTAIN BELLATEK TITANIUM ABUTMENT 5.0MM Reference Number: IEDAT5
    Category
    Medical Device
    Distribution
    11 states
  • LowFDA (Drugs)·D-0019-2021·2020-10-14

    VistaPharm Recalls Nystatin Oral Suspension Due to Impurity

    VistaPharm is recalling Nystatin Oral Suspension because one lot failed impurity specifications. The affected product was distributed nationwide.

    Product
    NYSTATIN ORAL SUSPENSION, USP 100,000 units per mL Contains: Alcohol 0.5% v/v (Bubblegum Flavored) 16 fl. oz. (480 mL) Manufactured by: VistaPharm, Inc. Largo FL 33771, USA NDC 66689-008-16 UPC 6668900816,
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0015-2021·2020-10-14

    Pharmaceutical Associates Recalls Citalopram Oral Solution Due to Impurities

    Pharmaceutical Associates Inc. is recalling Citalopram Oral Solution due to high impurity levels found during stability testing.

    Product
    Citalopram Oral Solution, USP 20 mg/10 mL, 10 mL unit dose cups, Rx Only, Mfg for: Pharmaceutical Associates, Inc. Greenville, SC 29605 NDC 0121-1696-40
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·20E077000·2020-10-13

    Diode Dynamics Recalls SL1 LED Headlamp Bulbs for Excessive Glare

    Diode Dynamics is recalling specific SL1 LED headlamp bulbs that exceed brightness standards and may cause glare to oncoming drivers, increasing crash risk.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V629000·2020-10-12

    Utilimaster Walk-In Van Recall for Throttle Pedal Interference

    Shyft Group is recalling 2020 Utilimaster Walk-In vans because the throttle pedal may get trapped by the floor tread plate, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide