State

New York product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35451–35475 of 86696

HighFDA (Devices)·Z-0893-2020·2020-02-05
Haemonetics Recalls CS Elite Processing Sets Due to Potential Bowl Cracks
Haemonetics is recalling CS Elite Processing Sets (125 ml) because cracks in the bowl core may cause fluid trapping and incomplete blood washing.
Product
CS Elite Processing Set (125 ml) Autotransfusion Device - Product Usage:its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0895-2020·2020-02-05
Haemonetics Recalls CS Elite Fastpack Autotransfusion Devices Due to Leak Risk
Haemonetics is recalling CS Elite Fastpack autotransfusion devices because cracks in the bowl core may cause leaks and incomplete blood washing.
Product
CS Elite Fastpack, 225 mL, 150 Res Autotransfusion Device - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0849-2020·2020-02-05
Vitreq Recalls VitreQ 23G Injection Needles Due to Sterility Concerns
Vitreq Bv is recalling VitreQ 23G PFC Injection Needles because microscopic tears in the sterile pouch may compromise sterility.
Product
VitreQ 23G PFC Injection Needle- Ref: MD23.D01 GTIN: 8719214221362
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0850-2020·2020-02-05
Vitreq Recalls VitreQ 25G Injection Needles Due to Sterility Concerns
Vitreq Bv is recalling VitreQ 25G PFC Injection Needles because microscopic tears in the sterile pouch may compromise sterility.
Product
VitreQ 25G PFC Injection Needle-Ref: MD25.D01 GTIN: 8719214221386
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0857-2020·2020-02-05
Vitreq Bv Recalls VitreQ 23G Pick Needles Due to Sterility Concerns
Vitreq Bv is recalling VitreQ 23G Pick Needles because microscopic tears in the sterile pouch may compromise sterility.
Product
VitreQ 23G Pick Needles-REF: CN23.D04 GTIN: 8719214221584
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0866-2020·2020-02-05
RayStation Treatment Planning Software Recalled for Dose Calculation Errors
RaySearch Laboratories is recalling RayStation software due to defects that may cause incorrect dose calculations during treatment planning.
Product
RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0867-2020·2020-02-05
Johnson & Johnson Recalls Healon GV PRO Ophthalmic Viscosurgical Devices
Johnson & Johnson is recalling Healon GV PRO ophthalmic viscosurgical devices because they may be difficult to remove from the eye, potentially causing increased pressure or equipment clogging.
Product
Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-0869-2020·2020-02-05
LivaNova Recalls Cyberonics VNS Therapy AspireSR Generators for Battery Depletion
LivaNova is recalling 745 Cyberonics VNS Therapy AspireSR Model 106 generators due to electrical leakage causing premature battery depletion.
Product
Cyberonics VNS Therapy AspireSR, Model 106 Generator, 26-0007-8400/1. The firm name on the label is CYBERONICS, INC., Houston, TX. Vagus nerve stimulator.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0897-2020·2020-02-05
Haemonetics Recalls Cell Saver 5/5+ and Elite Bowl Sets Due to Leak Risk
Haemonetics is recalling Cell Saver 5/5+ and Elite bowl sets because potential leaks may trap fluid, causing incomplete washing of recovered blood.
Product
JAPAN LOW VOL(125ML) CS5 SET,LN 261J - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma. The recovered blood is processed by a centrifugation and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0904-2020·2020-02-05
Haemonetics Recalls Cell Saver Elite Sets Due to Potential Bowl Cracks
Haemonetics is recalling Cell Saver Elite sets because cracks in the bowl core may trap fluid, causing incomplete washing of recovered blood.
Product
JAPAN CELL SAVER ELITE SET - 225ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and pumping this…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0902-2020·2020-02-05
Haemonetics Recalls Cell Saver Elite Fastpacks Due to Potential Bowl Cracks
Haemonetics is recalling Cell Saver Elite Fastpacks because cracks in the bowl core may cause fluid trapping and incomplete blood washing.
Product
JAPAN CS ELITE FASTPACK, 225ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and pumping this processed…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0856-2020·2020-02-05
Vitreq Bv Recalls VitreQ 25G Silicone Tipped Cannula Due to Sterility Concerns
Vitreq Bv is recalling VitreQ 25G Silicone Tipped Cannulas because microscopic tears in the sterile pouch may compromise sterility.
Product
VitreQ 25G Silicone Tipped Cannula-REF: CN25.D01 GTIN: 8719214221522
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0858-2020·2020-02-05
Vitreq Bv Recalls VitreQ 25G Pick Needles Due to Sterility Concerns
Vitreq Bv is recalling VitreQ 25G Pick Needles because microscopic tears in the sterile pouch may compromise sterility.
Product
VitreQ 25G Pick Needles-REF: CN25.D04 GTIN: 8719214221607
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0899-2020·2020-02-05
Haemonetics Recalls Japan Disp Sets Due to Potential Bowl Cracks
Haemonetics is recalling specific Japan Disp Sets for Cell Saver systems due to potential bowl cracks that may cause leaks and incomplete blood washing.
Product
JAPAN DISP SET, 261J, 205J, 208 - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma. The recovered blood is processed by a centrifugation and washing…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0906-2020·2020-02-05
Haemonetics Recalls Japan DISP SETs Due to Potential Bowl Cracks
Haemonetics is recalling 1,584 Japan DISP SETs because cracks in the bowl core may cause leaks and incomplete washing.
Product
Japan DISP SET, 263J, 205J, HAR - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0861-2020·2020-02-05
Vitreq 27G Blunt Needles Recalled for Potential Sterility Compromise
Vitreq Bv is recalling VitreQ 27G Blunt Needles because microscopic tears in the sterile pouch may compromise sterility.
Product
VitreQ 27G Blunt Needles with luer-lock connector-REF: CN27.D05 GTIN:8719214221669
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0853-2020·2020-02-05
Vitreq Recalls VitreQ 27G Cannulas Due to Sterility Concerns
Vitreq Bv is recalling VitreQ 27G VFI Cannulas because microscopic tears in the sterile pouch may compromise sterility.
Product
VitreQ 27G VFI Cannula-REF: CN27.D03 GTIN: 8719214221461
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0860-2020·2020-02-05
Vitreq Bv Recalls VitreQ 25G Blunt Needles Due to Sterility Concerns
Vitreq Bv is recalling VitreQ 25G Blunt Needles because microscopic tears in the sterile pouch may compromise sterility.
Product
VitreQ 25G Blunt Needles with luer-lock connector-REF : CN25.D05 GTIN: 8719214221645
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0846-2020·2020-02-05
Vitreq 23G Needles Recalled for Potential Sterility Compromise
Vitreq Bv is recalling VitreQ 23G needles because microscopic tears in the sterile pouch may compromise sterility.
Product
(1) VitreQ 23G BF Blunt Needles-BF23.D51 GTIN#: 8719214221126 (2) VitreQ 23G BF Brush Needles-BF23.D52 GTIN#: 8719214221140
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0888-2020·2020-02-05
Haemonetics Recalls Cell Saver 5/5+ Fastpacks Due to Potential Bowl Cracks
Haemonetics is recalling Cell Saver 5/5+ Fastpacks because cracks in the bowl core may cause fluid trapping and incomplete washing.
Product
CS5/5+ Fastpacks, 125 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0922-2020·2020-02-05
Roche Cobas infinity Software Recalled for Incorrect Alarm Mapping
Roche Diagnostics is recalling 20 Cobas infinity software modules due to incorrect alarm mapping. The software versions 2.4.1 through 2.5.4 are affected.
Product
Cobas infinity central lab / cobas infinity core license-a Calculator/Data Processing Module, For Clinical Use Material Number: 07154003001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0896-2020·2020-02-05
Haemonetics Recalls CS Elite Fastpack Autotransfusion Devices Due to Leak Risk
Haemonetics is recalling CS Elite Fastpack autotransfusion devices because cracks in the bowl core may cause leaks and incomplete washing.
Product
CS Elite Fastpack, 125 mL, 150 Res Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0854-2020·2020-02-05
Vitreq Recalls VitreQ 20G VFI Cannulas Due to Sterility Concerns
Vitreq Bv is recalling VitreQ 20G VFI Cannulas because microscopic tears in the sterile pouch may compromise sterility.
Product
VitreQ 20G VFI Cannula-REF: CN20.D03 GTIN: 8719214221485
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0917-2020·2020-02-05
Bard Conquest 40 PTA Dilation Catheter Recalled for Packaging Error
Bard Peripheral Vascular Inc. is recalling 286 units of Conquest 40 PTA Dilation Catheters because packaging incorrectly listed the balloon size, posing a risk of vessel injury.
Product
Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire .035"; Recommended Introducer 6F; Nominal Pressure 8atm, Rated Burst Pressure 40atm; Syringe inflation 1cc; UDI: (01)00801741060533(17)220228(10)REDQ3444
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-0891-2020·2020-02-05
Haemonetics Recalls Cell Saver 5/5+ Bowl Kits Due to Leak Risk
Haemonetics is recalling Cell Saver 5/5+ Bowl Kits because they may leak, trapping fluid and causing incomplete washing.
Product
Cell Saver¿5/5+ Bowl Kit (225 ml) Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.
Category
Medical Device
Distribution
Distributed nationwide