State

New York product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33251–33275 of 86693

HighFDA (Devices)·Z-2438-2020·2020-07-08
Siemens Atellica Data Manager Software Recalled for Potential Erroneous Patient Results
Siemens Healthcare Diagnostics is recalling Atellica Data Manager software versions 1.0 and 1.1 because unexpected interface driver behavior may cause quality control results to be assigned to incorrect control lot numbers, potentially leading to the reporting of erroneous patient results.
Product
(1) Atellica Data Manager software version 1.0 Siemens Material Number (SMN): 11314237 (2) Atellica Data Manager software version 1.1 Siemens Material Number (SMN): 11316888 Product Usage: are clinical laboratory information modules which consolidate test orders and test…
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-07082020-01·2020-07-08
BrucePac Recalls Diced Chicken Products Due to Undeclared Soy Allergen
BrucePac issued a public health alert for ready-to-eat diced chicken products distributed in Fort Worth, Texas, due to potential cross-contamination with soy, an undeclared allergen.
Product
BrucePac — FSIS Issues Public Health Alert for Ready-To-Eat Diced Chicken Products Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
HighCPSC·20147·2020-07-08
Pranarom Recalls Wintergreen Essential Oils for Packaging Safety Defect
Pranarom is recalling wintergreen essential oils because the packaging is not child-resistant, posing a poisoning risk to young children.
Product
Pranarom Wintergreen Essential Oils
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2449-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Potential Barrier Breach
LivaNova USA Inc. is recalling 648 units of Sterile Disposable Connectors because internal tests found the sterile barrier may be breached.
Product
Sterile Disposable Connectors ASY ASY STR CONN 3/8 STRLE 24 REF/ GTIN for Insert Label:050506000/ 00803622123238
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2471-2020·2020-07-08
Fujifilm Synapse PACS Software Recalled for Incorrect Orientation Markers
Fujifilm is recalling Synapse PACS Software versions 5.5.x and 5.7.x because incorrect orientation markers and slice locations may lead to misdiagnosis.
Product
Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as interface to the FUJIFILM Synapse PACS Software (Server)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2448-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling specific lots of sterile disposable connectors because internal tests found potential breaches in the sterile barrier.
Product
Sterile Disposable Connectors ASY S CONN 3/16X1/8 RDR ANLD24 REF/ GTIN for Insert Label:050513000/ 00803622123252
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2473-2020·2020-07-08
Elekta Unity Radiation Therapy System Recalled for Heating Issues
Elekta, Inc. is recalling 21 Unity Image-Guided Radiation Therapy Systems due to reports of excessive heating in the MRL Gradient Connection Module.
Product
Elekta Unity, Image-Guided Radiation Therapy System
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-2444-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling specific lots of Sterile Disposable Connectors because internal tests identified potential breaches in the sterile barrier.
Product
Sterile Disposable Connectors ASY 3/16 X 3/16 STR CONNW/LL24. REF/ GTIN for Insert Label:050432000 / 00803622123184
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2454-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling 744 units of sterile disposable connectors because internal tests found potential breaches in the sterile barrier.
Product
Sterile Disposable Connectors ASY Y CONN 1/4 X 1/4 X 1/4 24 REF/ GTIN for Insert Label:050524000/ 00803622123306
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2467-2020·2020-07-08
Radiometer ABL80-FLEX Box Label Recall for Barcode Misinterpretation Risk
Radiometer Medical ApS is recalling ABL80-FLEX box labels because barcode misinterpretation on analyzers may cause patient mix-ups or delayed treatment.
Product
ABL80-FLEX-393-839 Box Label, REF 393-839, IVD, CE, UDI: 05700693938394 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care setting.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2446-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling specific lots of Sterile Disposable Connectors because internal tests found potential breaches in the sterile barrier.
Product
Sterile Disposable Connectors ASY STR CONN 3/16 STRLE 24. REF/ GTIN for Insert Label:050503000/ 00803622123214
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2441-2020·2020-07-08
Mediana Attendant Vital Signs Monitor Recalled for Temperature Measurement Failures
Mediana Co., Ltd. is recalling 180 Attendant Vital Signs Monitors because failures were found in the temperature measurement function while in predict mode.
Product
DIRECT SUPPLY Attendant VITAL SIGNS MONITOR, REF AVSM2 - Product Usage: It is vital sign monitor to monitor noninvasive blood pressure (NIBP), functional arterial oxygen saturation (SpO2), pulse rate (PR), temperature (Temp) for adult, pediatric and neonatal patients in all…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2464-2020·2020-07-08
LivaNova Recalls Vein Irrigation Cannulas Due to Sterile Barrier Breach
LivaNova is recalling 325 Vein Irrigation Cannulas because internal tests found potential breaches in the sterile barrier, which could compromise sterility.
Product
Vein Irrigation Cannula with blunt tip. ASY VIC, STERILE 25/CS REF/ GTIN for Insert Label: VIC/ 00803622133107
Category
Medical Device
Distribution
44 states
ModerateFDA (Devices)·Z-2435-2020·2020-07-08
Westmed Recalls Neo-Vent Infant T-Piece Resuscitation Circuits Due to Fit Issues
Westmed, Inc. is recalling Neo-Vent Infant T-Piece Resuscitation Circuits because a mold repair resulted in non-compliant 15mm OD connections that prevent use with compatible infant resuscitators.
Product
Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask; Circuit for use on compatible Infant Resuscitators. 15mm OD x 10mm ID connector; REF 0420, Qty:10, Length: 60" (1.5cm), Rx Only.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2482-2020·2020-07-08
Ortho VITROS 5600 Software Recall for Parameter Reset Defect
Ortho Clinical Diagnostics is recalling VITROS 5600 Integrated System software versions 3.3.3 and below because assay parameters may reset to defaults.
Product
VITROS 5600 Integrated System Software Versions 3.3.3 and below Product Code: 6802413 Unique Identifier: 10758750002740
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1361-2020·2020-07-08
Children's Robitussin DM Recalled for Missing Dosing Cup Graduations
Glaxosmithkline is recalling 132,336 bottles of Children's Robitussin DM because the included dosing cups lack age-specific measurement markings.
Product
CHILDRENS ROBITUSSIN HONEY COUGH AND CHEST CONGESTION DM — CHILDRENS ROBITUSSIN HONEY COUGH AND CHEST CONGESTION DM (DEXTROMETHORPHAN HBR, GUAIFENESIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2484-2020·2020-07-08
Ortho VITROS XT 7600 Software Recall for Parameter Reset Issue
Ortho Clinical Diagnostics is recalling VITROS XT 7600 Integrated System software versions 3.5.1 and below because MicroWell Qualitative Assay parameters may reset to defaults.
Product
VITROS XT 7600 Integrated System Software Versions 3.5.1 and below Product Code:6844461 Unique Identifier: 10758750031610
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1376-2020·2020-07-08
Flexion Recalls Zilretta Injectable Suspension Due to Temperature Abuse
Flexion Therapeutics is recalling 792 kits of Zilretta (triamcinolone acetonide) because the product was stored at room temperature for more than six weeks.
Product
Zilretta (triamcinolone acetonide extended-release injectable suspension), 32mg per vial, 5mL vials, Single-dose Kits, Rx Only, Manufactured for: Flexion Therapeutics, Inc. 10 Mall Road, Suite 301, Burlington, MA 01803, NDC 70801-003-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2481-2020·2020-07-08
Ortho VITROS 3600 System Recalled for Assay Parameter Reset Issue
Ortho Clinical Diagnostics is recalling 27 refurbished VITROS 3600 Immunodiagnostic Systems because assay parameters may reset to defaults, potentially affecting test results.
Product
VITROS 3600 Immunodiagnostic System - Refurbished Product Code: 6802914 Unique Identifier: 10758750007103
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1362-2020·2020-07-08
Children's Dimetapp Cold & Cough Recalled for Missing Dosing Cup Graduations
Glaxosmithkline is recalling Children's Dimetapp Cold & Cough bottles because the included dosing cups are missing graduation marks for certain age groups.
Product
Childrens Dimetapp Cold & Cough, For ages 6 yrs. & over, 8 FL OZ. bottle, (237 mL), Distributed by: Pfizer Madison, NJ 07940, Made in Canada, UPC: 60300312234196, NDC: 0031-2234-19.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2483-2020·2020-07-08
Ortho VITROS 5600 System Recall for Software Parameter Reset Issue
Ortho Clinical Diagnostics is recalling 130 refurbished VITROS 5600 Integrated Systems because software modifications to assay parameters may be inadvertently reset to default.
Product
VITROS 5600 Integrated System - Refurbished Software Versions 3.3.3 and below Product Code: 6802915 Unique Identifier: 10758750007110
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2434-2020·2020-07-08
Westmed Recalls Neo-Vent Infant T-Piece Resuscitation Circuits Due to Fit Issues
Westmed, Inc. is recalling Neo-Vent Infant T-Piece Resuscitation Circuits because a manufacturing error resulted in non-compliant 15mm OD connections, preventing use with compatible infant resuscitators.
Product
Neo-Vent Infant T-Piece Resuscitation Circuit;Circuit for use on compatible Infant Resuscitators. 15mm OD x 10mm ID connector; REF 0415, Qty:10, Length: 60" (1.5cm), Rx Only.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2480-2020·2020-07-08
Ortho VITROS 3600 Software Recall for Parameter Reset Issue
Ortho Clinical Diagnostics is recalling VITROS 3600 Immunodiagnostic System software versions 3.3.3 and below because MicroWell Qualitative Assay parameters may reset to defaults.
Product
VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below Product Code: 6802783, Unique Identifier: 10758750002979
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2436-2020·2020-07-08
Westmed Neo-Vent Infant T-Piece Resuscitation Circuit Recall for Non-Compliant Connections
Westmed is recalling Neo-Vent Infant T-Piece Resuscitation Circuits because a mold repair resulted in non-compliant 15mm OD connections, preventing use with compatible infant resuscitators.
Product
Neo-Vent Infant T-Piece Resuscitation Circuit With Neonatal Mask; Circuit for use on compatible Infant Resuscitators. 15mm OD x 10mm ID connector; REF 0421, Qty:10, Length: 60" (1.5cm), Rx Only.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V398000·2020-07-07
Keystone Recalls Fifth-Wheel Trailers Due to Antenna Separation Risk
Keystone is recalling 2019-2020 fifth-wheel trailers because the television antenna may detach during transit, creating a road hazard.
Product
KEYSTONE — KEYSTONE CARBON, COUGAR, RAPTOR, FUZION
Category
Vehicle
Distribution
Distributed nationwide