State

New York product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51101–51125 of 86783

HighFDA (Devices)·Z-2152-2017·2017-06-07
Hans Pausch Uroview FD Fluoroscopic X-ray System Recalled for Footswitch Safety Issue
Hans Pausch is recalling 10 Uroview FD fluoroscopic X-ray systems because the footswitch used to activate radiation is part of the safety circuit.
Product
Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040 Primarily for urological applications (functional X-ray diagnostics, endourology and minimal invasive urology / surgery). The system, which includes a radiologic / urologic treatment table, maybe used…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2215-2017·2017-06-07
Zimmer Biomet Recalls AFFIXUS Hip Fracture Nail Due to Sizing Defect
Zimmer Biomet is recalling 33,500 AFFIXUS Hip Fracture Nail units worldwide because certain undersized specifications may prevent the nail from properly engaging with the targeting jig.
Product
AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric fractures, interochanteric fractures, high subtrochanteric fractures and combinations of these fractures…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·17173·2017-06-07
Madison Mill Recalls Foldaway Safety Gates Due to Entrapment Hazards
Madison Mill is recalling foldaway expandable safety gates because a child's neck can fit into the top opening, posing strangulation risks.
Product
Foldaway expandable safety gates
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2173-2017·2017-06-07
Roche Recalls PreciControl Varia 3 Due to Typographical Error
Roche Diagnostics is recalling 1,603 units of Elecsys PreciControl Varia 3 because the e-barcode and value sheet contain a typographical error for PTH target values.
Product
Elecsys PreciControl Varia 3
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2177-2017·2017-06-07
AbbVie Recalls PEG Kits Due to Missing or Duplicate Components
AbbVie is recalling specific lots of PEG Kits due to potential defects including missing components, duplicate parts, or missing labels and instructions.
Product
AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2109-2017·2017-06-07
Toshiba Angio WorkStation Recalled for Dose Tracking Display Error
Toshiba is recalling 70 Angio WorkStation units because the Peak Skin Dose value may display incorrectly if the workstation is powered on after the Infinix system.
Product
Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F
Category
Medical Device
Distribution
28 states
ModerateFDA (Devices)·Z-2166-2017·2017-06-07
Siemens SHBG Immulite 2000 Reagent Recall Due to Stability Issues
Siemens is recalling certain lots of SHBG Immulite 2000 reagents because they may not meet stability claims, potentially causing test bias.
Product
SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic use with the IMMULITE 2000 Systems Analyzers-For the quantitative measurement of SHBG in serum, as aid in the differential diagnosis of hirsutism.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2165-2017·2017-06-07
Pointe Scientific Lactate Dehydrogenase Reagent Set Recalled for Stability Issues
Medtest Holdings is recalling Pointe Scientific Lactate Dehydrogenase Reagent Sets because the product's stability claim is not being met.
Product
Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set Model Number(s): L7572. For the in vitro quantitative kinetic determination of lactate dehydrogenase activity in serum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2209-2017·2017-06-07
Cell Marque Recalls CD117 Reagents Due to Missing Export Labeling
Cell Marque is recalling CD117, c-kit reagents because they were not labeled 'For Export Only' as required by the FD&C Act.
Product
CD117, c-kit (YR145) 1.0 ml catalog number 117R-16 7.0 ml catalog number-18 Microbiology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2197-2017·2017-06-07
Acumed Recalls Slide-Loc Anatomic Radial Head System Due to Performance Issues
Acumed LLC is voluntarily removing the Slide-Loc Anatomic Radial Head System from the market due to complaints about instrumentation performance, trial design, and implant dissociations.
Product
The Acumed Slide-Loc Anatomic Radial Head System is intended for use by surgeons with orthopedic training. The device is to be implanted by the surgeon in a sterile operating room setting. Implants are provided in sterile packages. The Acumed Anatomic Radial Head Slide-Loc…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0869-2017·2017-06-07
VistaPharm Recalls Nystatin Oral Suspension Due to Impurity
VistaPharm is recalling Nystatin Oral Suspension because it contains an impurity peak that exceeds approved specifications.
Product
Nystatin Oral Suspension, USP, 100,000 units/mL, packaged in a) 2 fl.oz. (60mL) bottles (NDC 66689-008-02), and 500,000 units/5mL individual unit dose cup (NDC 66689-037-01) packaged in b) 50 count unit dose cups/case (NDC 66689-037-50) and c) 100 count unit dose cups/case (NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2216-2017·2017-06-07
Zimmer Biomet Recalls Modular Hybrid Glenoid Base for Quality Issues
Zimmer Biomet is voluntarily recalling 16 units of the Modular Hybrid Glenoid Base Large after two pieces with quality defects were shipped.
Product
Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System, The product is placed into an AlOx coated PET pouch and vacuum sealed with an Argon flush. The vacuum sealed product is then placed into a Tyvek/film pouch and that pouch is heat sealed. The fully pouched…
Category
Medical Device
Distribution
10 states
ModerateFDA (Devices)·Z-2178-2017·2017-06-07
AbbVie Recalls PEG Kits Due to Missing or Duplicate Components
AbbVie is recalling 3,331 PEG kits distributed in the US and 31 other countries because they may have missing components, duplicate parts, or missing labels.
Product
AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0880-2017·2017-06-07
Saphris Asenapine Tablets Recalled for Labeling Mixup
Forest Laboratories is recalling Saphris (asenapine) sublingual tablets because blister packs labeled as 10 mg actually contain 5 mg tablets.
Product
SAPHRIS — SAPHRIS (ASENAPINE MALEATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2169-2017·2017-06-07
Tosoh Bioscience Recalls AIA-PACK TgAb Control Set Due to Labeling Error
Tosoh Bioscience is recalling 64 boxes of AIA-PACK TgAb Control Set because the labels included instructions for a non-FDA approved methodology.
Product
AIA-PACK TgAb CONTROL SET
Category
Medical Device
Distribution
8 states
LowFDA (Devices)·Z-2210-2017·2017-06-07
Cell Marque Recalls HHV-8 Reagent Due to Export Labeling Error
Cell Marque is recalling HHV-8 in vitro diagnostic reagents because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Product
HHV-8 (13810); 1.0 ml catalog number 265M-16; 7.0 ml catalog number-265M-18; Microbiology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2203-2017·2017-06-07
Cell Marque Recalls Her2/Neu Reagent Due to Missing Export Labeling
Cell Marque is recalling Her2/Neu (c-erbB-2) reagents because they were not labeled as 'For Export Only' as required by law.
Product
Her2/Neu (c-erbB-2) (CB-1 1); 7.0 mL Catalog number 237M-18. In vitro diagnostic use - Analyte Specific Reagent Immunology - Analyte Specific Reagent
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2208-2017·2017-06-07
Cell Marque Recalls Varicella Zoster Virus Reagent Due to Labeling Error
Cell Marque is recalling Varicella Zoster Virus reagents because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Product
Varicella Zoster Virus 7.0 ml catalog number 364M-18 Microbiology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2204-2017·2017-06-07
Cell Marque Recalls Her2/Neu Reagents for Missing Export Labeling
Cell Marque is recalling Her2/Neu (EP3) reagents because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Product
Her2/Neu (EP3); 0.5 mL Catalog number 237R-25; 1.0 mL Catalog number 237R-26; 7.0 mL Catalog number 237R-28. Immunology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2205-2017·2017-06-07
Cell Marque Recalls Herpes Simplex Virus I Reagents Due to Labeling Error
Cell Marque is recalling Herpes Simplex Virus I reagents because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Product
Herpes Simplex Virus I; 7.0 mL Catalog number 361A-18. Microbiology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0868-2017·2017-06-07
Sandoz Recalls Subpotent Amoxicillin and Clavulanate Potassium Tablets
Sandoz Inc is recalling 4,464 bottles of Amoxicillin and Clavulanate Potassium tablets found to be subpotent in clavulanic acid.
Product
AMOXICILLIN AND CLAVULANATE POTASSIUM — AMOXICILLIN AND CLAVULANATE POTASSIUM (AMOXICILLIN AND CLAVULANATE POTASSIUM)
Category
Drug
Distribution
2 states
LowFDA (Devices)·Z-2201-2017·2017-06-07
Cell Marque Recalls Estrogen Reagent Due to Missing Export Labeling
Cell Marque is recalling 8 units of Estrogen Receptor reagent because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Product
Estrogen Receptor (SP1) 7.0 mL Catalog number 249R-18; Hematology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2202-2017·2017-06-07
Cell Marque Recalls H. pylori Reagent Due to Missing Export Labeling
Cell Marque is recalling five units of H. pylori reagent because they were not properly labeled as 'For Export Only' as required by the FD&C Act.
Product
H. pylori (polyclonal} 1.0 mL Catalog number 215A-76; Hematology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2207-2017·2017-06-07
Cell Marque Recalls SV40 Reagent Due to Missing Export Labeling
Cell Marque is recalling three units of SV40 (MRQ-4) reagent because they were not labeled 'For Export Only' as required by law.
Product
SV40 (MRQ-4) 0.5 ml catalog number 351 M-15. Microbiology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2168-2017·2017-06-07
Tosoh AIA-PACK TPOAb Control Set Recalled for Labeling Errors
Tosoh Bioscience is recalling 15 boxes of AIA-PACK TPOAb Control Sets because the labels included instructions for a non-FDA approved methodology.
Product
AIA-PACK TPOAb CONTROL SET
Category
Medical Device
Distribution
8 states