State

New York product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40026–40050 of 86762

ModerateFDA (Devices)·Z-1377-2019·2019-05-29
Remel Thio Med w/Dex, Hem, Vit K Media Recalled for Performance Failure
Remel Inc is recalling 8,615 units of Thio Med w/Dex, Hem, Vit K media due to potential performance failures starting 57 days after manufacturing.
Product
Thio Med w/Dex, Hem, Vit K (5ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1372-2019·2019-05-29
Polymer Technology Systems Recalls Lipid Panel Test Strips for Fit Issues
Polymer Technology Systems is recalling certain Lipid Panel test strips because they may not fit tightly into the optical block, potentially causing incorrect test results.
Product
Lipid Panel test strips (as a component of smart bundles), REF 2729, also private labeled under Henry Schein as REF 570-0412
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1379-2019·2019-05-29
Remel Thio Med w/Dex, Hem, Vit K Media Recalled for Performance Failure
Remel Inc is recalling Thio Med w/Dex, Hem, Vit K media because it may fail performance testing after 57 days. The expiration date is shortened to 56 days.
Product
Thio Med w/Dex, Hem, Vit K (7ml) 20/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1461-2019·2019-05-29
Zimmer GmbH Recalls Cannulated Orthopedic Screws Due to Material Concerns
Zimmer GmbH is recalling specific cannulated orthopedic screws because they may have been manufactured from a material different from the specifications.
Product
CBS high, countersink, cannulated, AO, Item Number 503004542
Category
Medical Device
Distribution
42 states
ModerateFDA (Drugs)·D-1294-2019·2019-05-29
Mallinckrodt Recalls Amitiza Capsules Due to Labeling Mix-Up
Mallinckrodt Pharmaceuticals is recalling Amitiza (lubiprostone) capsules because 8 mcg and 24 mcg bottles were found with incorrect contents.
Product
AMITIZA — AMITIZA (LUBIPROSTONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1387-2019·2019-05-29
KaVo Recalls DEXIS Titanium Intraoral Sensors Due to Calibration Error
KaVo Dental Technologies is recalling 211 DEXIS Titanium Intraoral Sensors because incorrectly programmed calibration files may reduce image quality.
Product
DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is intended to acquire dental intraoral radiographic images. The DEXIS / KaVo sensor shall be operated by healthcare professionals, who are educated and competent…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1456-2019·2019-05-29
Zimmer GmbH Recalls Cannulated Orthopedic Screws Due to Material Concerns
Zimmer GmbH is recalling specific cannulated orthopedic screws because an investigation found they may have been manufactured from a different material than specified.
Product
CBS high, countersink, cannulated, round-shaft, Item Number 503004342
Category
Medical Device
Distribution
42 states
ModerateFDA (Devices)·Z-1406-2019·2019-05-29
Remel Thio Med w/Dex, Hem, Vit K Media Recalled for Performance Failure
Remel Inc is recalling 1,069 units of Thio Med w/Dex, Hem, Vit K media due to potential performance failures after 106 days.
Product
Thio Med w/Dex, Hem, Vit K (10ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1370-2019·2019-05-29
Cook Stent Sets Recalled for Missing Warning About Stent Knotting
Cook Inc. is recalling Kwart RetroInject and Salle Intraoperative Pyeloplasty Stent Sets because the instructions for use did not include a warning for stent knotting.
Product
Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN: 4.0 Fr - SIPSF-040018-56-6 G18168 4.0 Fr - SIPSF-040018-59 G32773 4.7 Fr SIPSF-050018-59 G32774
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1447-2019·2019-05-29
Zimmer V-TEK IVP Step Drill Recalled for Material Specification Deviation
Zimmer GmbH is recalling V-TEK IVP step drills because they may have been manufactured from a material different from the applicable specifications.
Product
V-TEK", IVP step drill 2-3.4x124mm, 16mm stop, AO, Item Number 502015636
Category
Medical Device
Distribution
42 states
ModerateFDA (Devices)·Z-1380-2019·2019-05-29
Remel Thio Med w/Dex, Hem, Vit, K Media Recalled for Performance Failure
Remel Inc is recalling Thio Med w/Dex, Hem, Vit, K media because it may fail performance testing after 57 days. The expiration date is shortened to 56 days.
Product
Thio Med w/Dex, Hem, Vit, K (7ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1422-2019·2019-05-29
Zimmer GmbH Recalls 2.5x87mm AO Drills Due to Material Concerns
Zimmer GmbH is recalling specific AO drills because they may be made from the wrong material. The products were distributed to 38 US states.
Product
Drill, 2.5x87mm, AO, Item Number 502015137
Category
Medical Device
Distribution
42 states
ModerateFDA (Devices)·Z-1485-2019·2019-05-29
Zimmer GmbH Recalls 3.2x145mm AO Drills Due to Material Concerns
Zimmer GmbH is recalling specific AO drills because they may have been manufactured from a different material than specified.
Product
Drill, 3.2x145mm, AO, Item Number ST502015650
Category
Medical Device
Distribution
42 states
ModerateFDA (Devices)·Z-1414-2019·2019-05-29
Zimmer GmbH Recalls Drill Sys2.7 Due to Material Specification Deviation
Zimmer GmbH is recalling Drill Sys2.7 surgical instruments because they may have been manufactured from a material different from the defined specifications.
Product
Drill Sys2.7, 2x103mm, AO, Item Number 502015107
Category
Medical Device
Distribution
42 states
ModerateFDA (Devices)·Z-1404-2019·2019-05-29
Remel Thio Med Media Recalled for Potential Performance Failure
Remel Inc is recalling Thio Med w/o Ind, w/Dex media because it may fail performance testing after 106 days. The expiration date is being shortened to 105 days.
Product
Thio Med w/o Ind, w/Dex (10ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1280-2019·2019-05-29
Neusoft NeuViz 128 CT Scanner Recalled for Software Defect
Neusoft Medical Systems is recalling six NeuViz 128 CT scanners due to a software defect that may cause image loss during specific scans.
Product
NeuViz 128 Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x-ray system featuring a continuously rotating x-ray tube and detector array. The acquired x-ray transmission data is reconstructed by…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1279-2019·2019-05-29
Neusoft NeuViz 64 CT Scanner Recalled for Image Loss Defect
Neusoft Medical Systems is recalling 37 NeuViz 64 CT scanners due to a software defect that can cause image loss during specific scans.
Product
NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x-ray system featuring a continuously rotating x-ray tube and detector array. The acquired x-ray transmission data is reconstructed by…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1408-2019·2019-05-29
Remel Thio Med Culture Media Recalled for Potential Performance Failure
Remel Inc is recalling Thio Med culture media due to potential performance failures after 106 days. The expiration date is shortened to 105 days.
Product
Thio Med w/o Ind, w/Dex (18ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1469-2019·2019-05-29
Zimmer GmbH Recalls 2.7mm Orthopedic Drills Due to Material Concerns
Zimmer GmbH is recalling specific 2.7mm orthopedic drills because they may have been manufactured from a material different from the specifications.
Product
Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number ST502015207
Category
Medical Device
Distribution
42 states
ModerateFDA (Devices)·Z-1460-2019·2019-05-29
Zimmer GmbH Recalls CBS Micro Countersink Cannulated AO Screws
Zimmer GmbH is recalling CBS micro, countersink, cannulated, AO screws (Item Number 503004541) because they may have been manufactured from a different material than specified.
Product
CBS micro, countersink, cannulated, AO, Item Number 503004541
Category
Medical Device
Distribution
42 states
LowFDA (Devices)·Z-1389-2019·2019-05-29
Collagen Matrix Recalls Neomem Membrane Due to Incorrect Packaging
Collagen Matrix, Inc. is recalling Neomem Resorbable Collagen Membranes because they were packaged in the wrong box, potentially inside a Neomem FLEXPLUS box.
Product
Neomem Resorbable Collagen Membrane, 15 mm x 20 mm Reference Number (model): N1520 - Product Usage: Neomem is a bioresorbable, implantable collagen material that is intended for use in dental surgery procedures as a material for placement in the area of dental implant, bone…
Category
Medical Device
Distribution
Distributed nationwide
SevereUSDA FSIS·060-2019·2019-05-28
Richwell Group Recalls Frozen Siluriformes Fish Products for Import Violations
Richwell Group is recalling 160,020 pounds of frozen fish products imported from Vietnam without proper inspection. No illnesses have been reported.
Product
Richwell Group, Inc. Recalls Siluriformes Products Produced Without Benefit of Import Inspection
Category
Food
Distribution
Distributed nationwide
HighCPSC·19747·2019-05-28
Gildan Activewear Recalls Children's Sleep Sacks for Flammability Violation
Gildan Activewear is recalling American Apparel children's sleep sacks because they fail to meet federal flammability standards, posing a risk of burn injuries.
Product
Children's sleep sacks
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·19V393000·2019-05-24
Blue Bird Recalls Buses Due to Rear Brake Dragging Risk
Blue Bird is recalling certain 2015-2020 Vision and All American non-school buses because driver-side rear brakes may drag, posing a fire and injury risk.
Product
BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN, VISION TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V391000·2019-05-24
Blue Bird Recalls School Buses Due to Rear Brake Dragging Risk
Blue Bird is recalling 2015-2020 Vision and All American school buses because the driver-side rear brakes may drag, posing a fire and injury risk.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, ALL AMERICAN SCHOOL BUS, VISION TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide