State

New York product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29876–29900 of 86677

CriticalFDA (Food)·F-0345-2021·2021-03-31
El Abuelito Queso Fresco Recalled for Listeria Contamination Risk
El Abuelito Cheese, Inc. is recalling various brands of Queso Fresco due to potential Listeria monocytogenes contamination. The product was distributed in six states.
Product
Quseo Fresco sold under the following brands and container sizes - El Abuelito Cheese Brand - Queso Fresco Regular 12 oz.Plastic Container673130100003 Queso Fresco Promoci¿n 10 oz.Plastic Container673130100078 Queso Fresco de Hoja 12 oz.Plastic Container673130100065…
Category
Food
Distribution
6 states
CriticalFDA (Drugs)·D-0311-2021·2021-03-31
Adam's Secret Extra Strength 3000 Recalled for Unapproved Ingredients
The FDA is recalling Adam's Secret Extra Strength 3000 because it contains unapproved drugs tadalafil and sildenafil.
Product
Adam's Secret Extra Strength 3000, 840 mg, 10 count blister packs, Distributed by AS Inc., Made in USA, UPC 6 09728 43452 6.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0310-2021·2021-03-31
Adam's Secret Extra Strength Recalled for Unapproved Active Ingredients
Adam's Secret Extra Strength 1500 is being recalled because FDA analysis found unapproved drugs tadalafil and sildenafil in the product.
Product
Adam's Secret Extra Strength 1500, 800 mg, 10 count blister packs, Distributed by KP Inc., Made in USA, UPC 6 09728 43462 5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1284-2021·2021-03-31
Caire Diagnostics Recalls FenomPro Devices Due to Erroneous High FeNO Readings
Caire Diagnostics is recalling FenomPro devices because calibration drift and software errors may cause erroneously high FeNO readings, potentially leading to premature discontinuation of asthma treatment.
Product
CAIRE DIAGNOSTICS FenomPro REF 900-0001 SN ***** - Product Usage: a portable, non-invasive device to measure fractional exhaled nitric oxide (FeNO) in human breath. Fenom Pro should not be used in critical care, emergency care or in anesthesiology.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1280-2021·2021-03-31
Baxter Recalls Prismaflex Preventative Maintenance Kits Due to Tubing Performance Variability
Baxter Healthcare is recalling Prismaflex Preventative Maintenance Kits and spare part kits because tubing performance variability may cause alarms during or after system self-tests.
Product
Preventative Maintenance Kits G5010007) and spare part kits (G5064801 and G5006203) - Product Usage: For Prismaflex Control Units, used for Continuous Renal Replacement Therapy (CRRT).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0313-2021·2021-03-31
ICU Medical Recalls Sodium Chloride Irrigation Due to Particulate Matter
ICU Medical is recalling 425,628 bottles of 0.9% Sodium Chloride Irrigation due to the presence of particulate matter.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0346-2021·2021-03-31
El Abuelito Requeson Ricotta Recalled Due to Listeria Contamination Risk
El Abuelito Cheese, Inc. is recalling specific 12oz containers of Requeson Ricotta because the product may be contaminated with Listeria monocytogenes.
Product
Requeson/Ricotta, sold under the following brands and container sizes: El Abuelito Requeson Ricotta 12oz Clam Shell Container, UPC: 673130300014; El Abuelito Requeson Ricotta - Promocion $3.99 12oz. Clam Shell Container, UPC: 673130300014; El Viejito Requeson/Ricotta 12oz. Clam…
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-1282-2021·2021-03-31
Hitachi Arietta 850 Ultrasound System Recalled for Acoustic Output Error
Hitachi Medical Systems America Inc. is recalling Arietta 850 ultrasound systems with specific software versions due to an error that can cause acoustic output to exceed regulatory limits.
Product
Ultrasonic pulsed doppler imaging system - Product Usage: intended for use by trained personnel (doctor, Sonographer, etc.) for the diagnostic ultrasound evaluation of Fetal, Abdominal, Intra-operative (Spec.), Intraoperative (Neuro.), Laparoscopic, Pediatric, Small Organ…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1296-2021·2021-03-31
Getinge Operating Table System Recalled for Hydraulic Leakage Risk
Getinge Group Logistics America, LLC is recalling 4,288 Operating Table Systems due to a potential hydraulic leakage that could cause unintended table movement.
Product
Operating Table System
Category
Medical Device
Distribution
41 states
HighNHTSA·21V225000·2021-03-31
Harley-Davidson motorcycles recalled for faulty headlight bulbs and visibility loss
Harley-Davidson is recalling 2019-2021 Sportster motorcycles and replacement headlight assemblies because the glass bulb may fail, causing loss of both high and low beams and increasing crash risk.
Product
HARLEY-DAVIDSON — HARLEY-DAVIDSON XL1200NS, XL1200C, XL883N, XL883L
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V224000·2021-03-31
2021 Porsche Macan recalled for loose shock absorber screw connections
Certain 2021 Porsche Macan models have improperly tightened screw connections on shock absorbers, which could compromise braking and vehicle control. Porsche will repair the connections free of charge.
Product
PORSCHE — PORSCHE MACAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1297-2021·2021-03-31
Stryker S-Series Equipment Management System Recall for Brake Disengagement Risk
Stryker is recalling S-Series Equipment Management Systems because capacitive touch controls may disengage when electrocautery devices are in use.
Product
S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502 Components that are affected within the S-Series Finished Good Model Number o P38198 - ASM, MFR CONTROLLER, FIXED STANDARD o P38199 - ASM, MFR CONTROLLER, LIFT STANDARD o P40553 - ASM, MFR…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1292-2021·2021-03-31
Olympus Recalls TJF-Q190V Duodenoscopes Due to Reported Mucosal Injury
Olympus is recalling 1,564 TJF-Q190V duodenoscopes and accessories worldwide due to complaints of mucosal injury associated with the forceps elevator region.
Product
Duodenoscope and accessories, flexible/rigid - Product Usage: used with an Olympus video system center, light source, documentation equipment, monitor, Endo Therapy accessories (such as biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery within…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1281-2021·2021-03-31
RayCare 3B Oncology Software Recalled for Data Loss During Upgrade
RaySearch Laboratories AB is recalling RayCare 3B software because patient messages may be lost when upgrading from RayCare 2.
Product
RayCare 3B (3.1.0.60341) - Product Usage: Intended Use Oncology information system that supports healthcare professionals in delivering cancer care.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1294-2021·2021-03-31
Teleflex Recalls Rusch Polaris Laryngoscopes Due to Handle Cracking
Teleflex is voluntarily recalling Rusch Polaris laryngoscopes because customers reported that the handles develop cracks or break at the hinge.
Product
RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1298-2021·2021-03-31
Teleflex Recalls PLEUR-EVAC Thoracic Catheters Due to Sterility Concerns
Teleflex is recalling 520 PLEUR-EVAC Thoracic Catheters because the company cannot guarantee the devices are sterile.
Product
PLEUR-EVAC Thoracic Catheters (CATHETER, IRRIGATION). The thoracic catheter is a sterile, non pyrogenic, single use device that allows drainage from the mediastinum and/or the pleural space. The thoracic catheter is composed of Phthalate-free PVC material and is available in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1278-2021·2021-03-31
Baxter Recalls Prismaflex Control Units Due to Tubing Performance Variability
Baxter Healthcare is recalling 1,225 Prismaflex Control Units used for Continuous Renal Replacement Therapy because tubing performance variability may cause alarms during or after system self-tests.
Product
Prismaflex Control Unit - Product Usage: Used for Continuous Renal Replacement Therapy (CRRT).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1289-2021·2021-03-31
Bard Marquee Biopsy Instruments Recalled for Detaching Switch
Bard Peripheral Vascular Inc is recalling Marquee Disposable Core Biopsy Instruments because the penetration depth switch may detach during use.
Product
BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm, XX.Xcm, XXg x XXcm REF XXXXXXX Note - for definition of the "X's refer to Tyvek Lid Label.pdf" uploaded in Associated Documents
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-1299-2021·2021-03-31
Meridian ImmunoCard Mycoplasma EIA Recalled for Potential False-Negative Results
Meridian Bioscience is recalling 8 ImmunoCard Mycoplasma EIA kits due to incorrect storage that could cause false-negative or invalid results, potentially delaying appropriate patient treatment.
Product
The ImmunoCard Mycoplasma EIA detects the presence of IgM to M. pneumoniae in serum - Product Usage: intended to aid in the diagnosis of recent Mycoplasma pneumoniae infection.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1293-2021·2021-03-31
Mizuho Operating Table Hand Control Units Recalled for Sliding Risk
Mizuho OSI is recalling 26 operating table hand control units because they may cause the tabletop to slide in the opposite direction, potentially delaying surgical procedures.
Product
Mizuho CE IPX4, mode MOT-5602BW, 100-240, 50-60Hz, 400VA, REF 18-140-20 containing hand control Unit - Product Usage: intended to support a patient during surgical operations.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1283-2021·2021-03-31
In2Bones Shannon Percutaneous Burr Recalled for Potential Breakage During Use
In2Bones is recalling 60 units of Shannon Percutaneous Burrs due to manufacturing non-conformity that may cause the burr to break during surgery.
Product
In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percutaneous surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1290-2021·2021-03-31
Corin Trinity Hip Prosthesis Heads Recalled for Incorrect Size Labeling
Corin Ltd is recalling 23 units of Trinity Biolox Delta Ceramic Heads due to incorrect size labeling on packaging and patient stickers.
Product
Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1301-2021·2021-03-31
Cardinal Health Recalls In-View Clear Leggings Due to Manufacturing Variance
Cardinal Health is recalling In-View Clear Leggings because a manufacturing variance causes the product to stick, preventing proper application.
Product
In-View Clear Leggings Sterile Non-Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1304-2021·2021-03-31
Cardinal Health Recalls Femoral Angiography Drapes Due to Sticking Defect
Cardinal Health is recalling non-sterile femoral angiography drapes because a manufacturing defect causes them to stick, preventing proper application.
Product
Femoral Angiography Drape Bulk Non-Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1300-2021·2021-03-31
Cardinal Health Recalls In-View Clear Leggings Due to Manufacturing Variance
Cardinal Health is recalling In-View Clear Leggings Sterile because a manufacturing variance causes the plastic film to stick, potentially preventing proper application.
Product
In-View Clear Leggings Sterile
Category
Medical Device
Distribution
Distributed nationwide