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.

42501–42525 of 86765

SevereFDA (Drugs)·D-0276-2019·2018-11-21
Taro Recalls Children's Allergy Solution Due to Impurity
Taro Pharmaceuticals is recalling 12,432 bottles of Children's 24 Hour Allergy Oral Solution because an unknown impurity exceeded limits during stability testing.
Product
Children's 24 Hour Allergy (cetirizine hydrochloride) Oral Solution 1 mg/mL, Bubble Gum Flavor, Sugar Free/Dye Free, 4 FL OZ (120 mL) bottle, Dist. by Meijer Distribution, Inc., Grand Rapids, MI 40644, NDC 41250-106-08, UPC 7 13733 88578 2.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0620-2019·2018-11-21
Wegmans Pumpkin Loaf Recalled for Undeclared Milk Allergen
Wegmans Food Markets is recalling 19-ounce Pumpkin Loaf products due to undeclared milk. The recall affects Wegmans stores in six states.
Product
Wegmans Pumpkin Loaf, 19 oz., UPC 77890 27002
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-0426-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold mesh devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 18x22cm, Part Number F10256-1822G
Category
Medical Device
Distribution
8 states
SevereFDA (Food)·F-0697-2019·2018-11-21
Sirob Imports Recalls FC Finest Choice Hot Curry Powder for Lead
Sirob Imports, Inc. is recalling 12,100 pounds of FC Finest Choice Hot Curry Powder because the product may contain elevated levels of lead.
Product
FC Finest Choice Hot Curry Powder, Packed By SIROB IMPORTS, INC. packaged in a 50 pound box.
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0696-2019·2018-11-21
Sirob Imports Recalls Curry Powder Due to Elevated Lead Levels
Sirob Imports, Inc. is recalling various brands of curry powder because the products may contain elevated levels of lead.
Product
Curry powder packaged under bulk, retail, and food service labels. Bulk: CURRY POWDER Net Weight 55 LBS, DISTRIBUTED BY SIROB IMPORTS LINDENHURST, NEW YORK USA (sold in a 55 pound bag) Packaged under the following retail brands: Corrado 16 oz. UPC: 0 12729 01100…
Category
Food
Distribution
6 states
SevereFDA (Drugs)·D-0250-2019·2018-11-21
Kadesh Recalls Puriton Eye Relief Drops for Non-Sterility
Kadesh International is recalling Puriton Eye Relief Drops because they were manufactured under non-sterile production conditions.
Product
puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0450-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail Left 125 Deg 9x165mm, Item Number 816709165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V825000·2018-11-21
Great Dane Recalls 2019 Freedom Trailers Due to Narrow Rear Impact Guards
Great Dane Trailers is recalling 2019 Freedom Combo Drop Deck Platform trailers because the rear impact guards may be too narrow, potentially failing to prevent vehicles from going under the trailer in a crash.
Product
GREAT DANE — GREAT DANE FREEDOM
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0460-2019·2018-11-21
Virtual Imaging RadPRO Mobile X-Ray System Recalled for Mount Separation Risk
Virtual Imaging is recalling 253 RadPRO Mobile 40kW Digital X-Ray Systems because the tube head may separate and fall off the unit.
Product
RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product Usage: Instrument is used to take diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts on both adult and pediatric subjects. Applications…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0438-2019·2018-11-21
Stryker Spirit Plus Bed Recall for Potential Entrapment Risk
Stryker is recalling 20,030 Spirit Plus hospital beds with high rail siderails due to non-compliance with safety standards and a potential risk of patient entrapment.
Product
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Category
Medical Device
Distribution
50 states
HighFDA (Devices)·Z-0441-2019·2018-11-21
R82 A/S Recalls Heron Toilet and Bath Chairs Due to Aluminum Gas Spring
R82 A/S is recalling 687 Heron toilet and bath chairs because they contain aluminum gas spring heads. The recall is a replacement campaign for these specific units.
Product
Heron toilet and bath chair Model 880505-01 & 880505-11
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0425-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold 16x20cm devices because the PGA suture material degraded, causing them to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 16x20cm, Part Number F10256-1620G
Category
Medical Device
Distribution
8 states
HighFDA (Drugs)·D-0258-2019·2018-11-21
Sandoz Recalls Isosorbide Dinitrate Tablets Due to Cross Contamination
Sandoz Inc. is recalling 18,832 bottles of Isosorbide Dinitrate 20 mg tablets due to cross-contamination with other products.
Product
ISOSORBIDE DINITRATE — ISOSORBIDE DINITRATE (ISOSORBIDE DINITRATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0422-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 6x10cm, Part Number F10256-0610G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0442-2019·2018-11-21
Arthrex Recalls 3.2mm Proximal Reamer Due to Potential Breakage During Use
Arthrex, Inc. is recalling 832 units of the 3.2mm Proximal Reamer/Cannulated Drill because the instrument may break during use.
Product
3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail Procedure Pack: Contains instrumentation for the implantation of the FibuLock implant. Contents include: Actuation Driver, 6.2mm Reamer, 3.2mm Reamer, 2 mm Drill…
Category
Medical Device
Distribution
30 states
HighFDA (Devices)·Z-0451-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Malfunction
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 125 Deg 10x165mm, Item Number 816710165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0445-2019·2018-11-21
Luminex Recalls Verigene Blood Culture Gram-Positive Nucleic Acid Kits
Luminex Corporation is recalling 12,700 trays of Verigene Blood Culture Gram-Positive Nucleic Acid Kits due to a potential for false negative results.
Product
VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro diagnostic test for the simultaneous detection and identification of potentially pathogenic gram-positive bacteria.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0435-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications after 18 months.
Product
OviTex 2S Reinforced BioScaffold 10x12cm, Part Number F10258-1012G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0432-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold mesh devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 18x22cm, Part Number F10258-1822G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0469-2019·2018-11-21
Tosoh AIA-900 Analyzer Recalled Due to Pickup Arm Malfunction
Tosoh Bioscience is recalling 393 AIA-900 Analyzers because a pickup arm malfunction can stop the device from testing patient samples, causing delays in results.
Product
AIA-900 Analyzer, Product code 022930, 022930R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0449-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail Left 130 Deg 11x300mm, Item Number 814611300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0430-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material may degrade, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 10x20cm, Part Number F10258-1020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0424-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold mesh devices because the suture material degraded, causing some units to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 10x20cm, Part Number F10256-1020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0421-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold 4x8cm devices because the PGA suture material degraded, causing the devices to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 4x8cm, Part Number F10256-0408G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0418-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold mesh devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex Reinforced BioScaffold 10x20cm, Part Number F10254-1020G
Category
Medical Device
Distribution
8 states