State

New York product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46226–46250 of 86773

HighFDA (Devices)·Z-1280-2018·2018-04-11
Baxter Recalls Prismaflex Control Units Due to Software and Usage Issues
Baxter Healthcare is recalling 3,440 Prismaflex Control Units worldwide due to reports of operators failing to follow safe unloading instructions and software errors in specific versions.
Product
Prismaflex Control Unit. Dialyzer, high permeability with or without sealed dialysate system. Continuous Renal Replacement Therapy (CRRT) for patients weighing 20 kilograms or more with acute renal failure and/or fluid overload. *Therapeutic Plasma Exchange (TPE) therapy for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1307-2018·2018-04-11
C.R. Bard Recalls HydroSil Gripper Intermittent Catheters Due to Seal Defects
C.R. Bard is recalling specific lots of HydroSil Gripper Intermittent Catheters because some units were found caught in the sterile barrier seal or cut.
Product
HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual pouch. MGC3 Product Usage Intermittent catheters are intended for urinary bladder drainage in patients requiring catheterization for management of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1308-2018·2018-04-11
C.R. Bard Recalls Magic 3 Intermittent Catheters Due to Seal Defects
C.R. Bard is recalling Magic 3 Intermittent Catheters because some units were caught in the sterile barrier seal or cut.
Product
Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box, each catheter is packaged in an individual pouch. Urinary catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1293-2018·2018-04-11
GE Healthcare Recalls Monica IF24 Interface System Due to Signal Swap Risk
GE Healthcare is recalling 355 Monica IF24 Interface Systems because incorrectly reconnected cables can cause fetal and maternal heart rate signals to be displayed incorrectly.
Product
Uterine Electromyographic Monitor -Monica IF24 Interface System Product Usage: The Monica IF24 CTG Interface Device is an accessory to the Monica AN24 which provides a means of interfacing the wireless output of the Monica AN24 to the transducer inputs of a CTG Fetal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1309-2018·2018-04-11
C.R. Bard Recalls Personal Intermittent Catheters Due to Seal Defects
C.R. Bard is recalling Personal Intermittent Catheters because some units were found caught in the sterile barrier seal or cut.
Product
Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box, each catheter is packaged in an individual pouch, Item Numbers: 50612, 50614, 50616, 50618, 52306, 52308, 52310, 52606, 52606G, 52608, 52608G, 52610, 52610G, 53314, 53320, 53514G, 53610, 53610G…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1281-2018·2018-04-11
Arrow Radial Artery Catheterization Kits Recalled for Shelf Life Labeling Error
Arrow International is recalling 930 Radial Artery Catheterization Kits because the included povidone iodine prep pads are labeled with an incorrect 36-month shelf life instead of 24 months.
Product
Radial Artery Catheterization Kit; Model: AK-04018
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1302-2018·2018-04-11
GE Healthcare Recalls Centricity PACS-IW Due to Image Data Loss Risk
GE Healthcare is recalling 569 units of Centricity PACS-IW because a database error may cause image series to be missing from exams without user notification.
Product
GE Healthcare Centricity PACS-IW, Model Numbers: (a) 2052831-00X (b) 2049588-008 Product Usage: Centricity PACS-IW by GE Healthcare is a device that receives medical images (including mammograms) and data from various imaging sources. Images and data can be stored…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1277-2018·2018-04-11
Halyard Health Recalls CORTRAK 2 Nasogastric Feeding Tubes
Halyard Health is recalling CORTRAK 2 feeding tubes because the internal stylet may be visible in the exit port window, deviating from specifications.
Product
CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with Electromagnetic Transmitting Stylet and CORFLO* Enteral Feeding tube, ANTI-IV* Connector, 10 Fr, 140 cm The device is used in patients that require intermittent or continuous tube feedings via the nasogastric or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0616-2018·2018-04-11
Mayne Pharma Recalls Fabior Foam Due to Stability Test Failures
Mayne Pharma is recalling 3,312 cans of Fabior (tazarotene) Foam, 0.1%, because stability testing showed high out-of-specification results for the active ingredient.
Product
FABIOR — FABIOR (TAZAROTENE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1282-2018·2018-04-11
Arrow Radial Artery Catheterization Kits Recalled for Shelf Life Labeling
Arrow International is recalling Radial Artery Catheterization Kits because the included povidone iodine prep pads do not meet the 36-month shelf life requirement.
Product
Radial Artery Catheterization Kit; Model: AK-04020
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1283-2018·2018-04-11
Arrow Radial Artery Catheterization Kits Recalled for Shelf Life Labeling Error
Arrow International is recalling Radial Artery Catheterization Kits because the included povidone iodine prep pads do not meet the 36-month shelf life requirement and must be labeled with a 24-month shelf life.
Product
Radial Artery Catheterization Kit; Model: AK-04020-C
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1284-2018·2018-04-11
Arrow Radial Artery Catheterization Kits Recalled for Shelf Life Labeling Error
Arrow International is recalling Radial Artery Catheterization Kits because the included povidone iodine prep pads do not meet the 36-month shelf life requirement and should be labeled with a 24-month shelf life.
Product
Radial Artery Catheterization Kit; Model: AK-04120
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1306-2018·2018-04-11
Zimmer Biomet Recalls A.L.P.S. Calcaneus Locking Plate Guide Inserts
Zimmer Biomet is recalling 22 A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts due to incorrect color anodization.
Product
A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts, Item Number: 816209003,UDI: 00887868044670989403
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-1286-2018·2018-04-11
Arrow Radial Artery Catheterization Kits Recalled for Shelf Life Labeling
Arrow International is recalling Radial Artery Catheterization Kits because the included povidone iodine prep pads do not meet the 36-month shelf life requirement and should be labeled with a 24-month shelf life.
Product
Radial Artery Catheterization Kit; Model: AK-04220
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1287-2018·2018-04-11
Arrow Arterial Access Tray Recall for Povidone Iodine Shelf Life Labeling
Arrow International is recalling Arterial Access Trays because the included povidone iodine prep pads do not meet the 36-month shelf life requirement and must be labeled with a 24-month shelf life.
Product
Arterial Access Tray, introducer catheter; Model: GU-04020
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1313-2018·2018-04-11
Phadia Recalls ImmunoCAP Allergen c6 Amoxicilloyl Due to Stability Failures
Phadia US Inc is recalling 950 units of ImmunoCAP Allergen c6, Amoxicilloyl because the product failed to meet stability specifications.
Product
ImmunoCAP Allergen c6, Amoxicilloyl ( Article number 14-4451-016). ImmunoCAP Specific IgE is an in vitro quantitative assay for the measurement of allergen specific IgE in human serum or plasma; to be used with the instrument Phadia 250, Phadia 1000, Phadia 2500 and Phadia…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1285-2018·2018-04-11
Arrow Radial Artery Catheterization Kits Recalled for Shelf Life Labeling Error
Arrow International is recalling 570 Radial Artery Catheterization Kits because the included povidone iodine prep pads are labeled with an incorrect 36-month shelf life.
Product
Radial Artery Catheterization Kit; Model: AK-04122
Category
Medical Device
Distribution
Distributed nationwide
ModerateUSDA FSIS·032-2018·2018-04-11
Koch Foods Recalls Beef Patties Due to Plastic Contamination
Koch Foods is recalling approximately 119,480 pounds of beef rib-shaped patties that may contain thin blue plastic pieces. No adverse reactions have been reported.
Product
Koch Foods — Koch Foods Inc. Recalls Beef Products Due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1312-2018·2018-04-11
Phadia Recalls ImmunoCAP Allergen c5 Ampicilloyl Test Kits
Phadia US Inc is recalling ImmunoCAP Allergen c5, Ampicilloyl test kits because stability specifications were not met.
Product
ImmunoCAP Allergen c5, Ampicilloyl (article number 14-4450-01). ImmunoCAP Specific IgE is an in vitro quantitative assay for the measurement of allergen specific IgE in human serum or plasma. To be used with the instrument Phadia 250, Phadia 1000, Phadia 2500 and Phadia…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0618-2018·2018-04-11
InvaGen Recalls Bupropion Hydrochloride Tablets for Dissolution Failures
InvaGen Pharmaceuticals is recalling specific lots of Bupropion Hydrochloride Extended-Release Tablets because they failed dissolution specifications during stability testing.
Product
BUPROPION HYDROCHLORIDE (SR) — BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0619-2018·2018-04-11
InvaGen Recalls Bupropion Hydrochloride Tablets for Dissolution Failures
InvaGen Pharmaceuticals is recalling specific lots of Bupropion Hydrochloride Extended-Release Tablets because they failed dissolution specifications during stability testing.
Product
BUPROPION HYDROCHLORIDE (SR) — BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V226000·2018-04-10
Keystone Recalls 2018 Raptor and Carbon Trailers for Fuel Fire Risk
Keystone is recalling 2018 Raptor and Carbon fifth-wheel trailers because missing fuel barriers allow absorption into the floor, increasing fire risk.
Product
KEYSTONE — KEYSTONE RAPTOR, CARBON
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E023000·2018-04-10
SynTec Recalls S3B Restraint Wall Mounted Seats Due to Bracket Crack Risk
SynTec Seating Solutions is recalling S3B Restraint Wall Mounted Seats because the mounting bracket may crack, increasing injury risk in a crash.
Product
SEATS recall
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18735·2018-04-10
2017 Can-Am Outlander ATVs Recalled for Steering Shaft Crash Hazard
BRP is recalling 2017 Can-Am Outlander and Outlander Max ATVs because the dynamic power steering shaft can break, causing a loss of steering control and crash hazard.
Product
2017 Can-Am Outlander and Outlander Max All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V228000·2018-04-10
Indian Motorcycle Recalls 2018 Models Due to Unintended Starting Risk
Indian Motorcycle is recalling 3,341 2018 models because corrosion in the combination switch may cause the bike to start unintentionally, posing a carbon monoxide risk.
Product
INDIAN — INDIAN SPRINGFIELD DARK HORSE, CHIEF, CHIEF VINTAGE, CHIEFTAIN ELITE
Category
Vehicle
Distribution
Distributed nationwide