State

New York product recalls

73,104 recalls have nationwide distribution and so reach New York. 12,938 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,938
Critical: 1,511
Severe: 3,148
Most recent: 2026-09-25

Of the 12,938 recalls naming New York we have scored against our rubric, 1,511 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,148 (24%) are Severe.

Which agencies issued them

These figures cover only the 12,938 recalls whose distribution notice names New York specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11476–11500 of 86042

HighFDA (Devices)·Z-2437-2024·2024-07-31
Perfusor Space Syringe Pump Recalled for Monoject Syringe Incompatibility Risk
B Braun's Perfusor Space infusion pump may be incompatible with Cardinal Health Monoject syringes affected by manufacturing changes, creating risks of overdose, underdose, and delayed therapy.
Product
Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Non-Wireless Model/Catalog Number: 8713032U Product Description: Perfusor Space Syringe Pump, Non-Wireless, Infusion Pump, 1 each Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2414-2024·2024-07-31
Dxl 9000 Immunoassay Analyzer Recalled for Corrosion of USB Cable Contacts
Beckman Coulter is recalling 143 Dxl 9000 Immunoassay Analyzers due to nonconforming USB cables with brass instead of gold contacts. Brass may corrode, potentially disabling internal communication and delaying patient test results.
Product
Dxl 9000 Access Immunoassay Analyzer, Catalog #C11137.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2423-2024·2024-07-31
Medtronic TourniKwik Tourniquet Set Recalled for Incorrect Component
Medtronic is recalling 636 units of TourniKwik Tourniquet Sets due to incorrect components placed in four manufactured lots. Distribution includes the US states of Minnesota, Massachusetts, Utah, California, Florida, Japan, and Slovenia.
Product
TourniKwik Tourniquet Set (CFN 79012)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2418-2024·2024-07-31
Wireless Nurse Call Station Recalled for Potential Alarm Communication Failure
Arial Call Station wireless nurse call systems (models CSK200-1069 and CSK200-1069MR) are recalled due to risk of alarm communication failure and premature battery depletion. 77 units affected across multiple U.S. states.
Product
Arial Call Station, Model Numbers CSK200-1069 and CSK200-1069MR, is a wireless nurse call station.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-2428-2024·2024-07-31
Beckman Coulter Clinical Reagent Recalled Due to Incorrect Lipemia Check Settings
Beckman Coulter has recalled 13,565 units of IGM clinical reagent due to incorrect lipemia check settings that may produce false low results or report high results as normal. Affected units were distributed worldwide.
Product
Beckman Coulter, REF: OSR61173, IGM 4x14 mL R1, 4x11 mL R2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2427-2024·2024-07-31
Medtronic A610 Clinician Programmer pocket adaptors limited to head-only MRI
Medtronic recalled A610 Clinician Programmer software and pocket adaptors (Models 64001, 64002) due to MRI safety restrictions. Patients with these implants are limited to head-only MRI procedures.
Product
A610 Clinician Programmer (CP) Software Application (app) with the following versions: Version 2.0.x (2.0.4584, 2.0.4594, 2.0.4605, 2.0.4630, and 2.0.4648), Version 3.0.x (3.0.1057, 3.0.1062, 3.0.1081, and 3.0.1098), Version 4.0.x (4.0.1052). Includes the below product…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2436-2024·2024-07-31
Perfusor Space infusion pump syringe incompatibility may cause dosing error
B Braun is recalling Perfusor Space infusion pump kits because Cardinal Health Monoject syringes have manufacturing changes that make them incompatible, potentially causing overdose, underdose, or delayed therapy.
Product
Brand Name: Perfusor Space Product Name: PERFUSOR SPACE ACM-KIT Model/Catalog Number: 8713040U Product Description: Perfusor Space, Infusion Pump Kit, 1 each Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2433-2024·2024-07-31
Infusion Pump Syringe Compatibility Issue May Cause Overdose or Underdose
B Braun is recalling Perfusor Space infusion pumps due to syringe compatibility issues with Cardinal Health Monoject syringes. The incompatibility may cause overdose, underdose, therapy delays, and alarm failures.
Product
Brand Name: Perfusor Space Product Name: Perfusor Space Infusion Pump System Model/Catalog Number: 8713030U Product Description: Perfusor Space Infusion Pump System, Infusion Pump, 1 each Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2438-2024·2024-07-31
Sensis Vibe diagnostic systems software crash during event documentation
Siemens Sensis Vibe diagnostic systems may crash when using documentation features during once-per-study event reporting. Three systems are affected; no injuries reported.
Product
Sensis Vibe systems with software version VD15B in combination with Sensis High End Server -Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology as…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2424-2024·2024-07-31
BD Nano 2nd Gen Pen Needles recalled for post-expiration distribution
Embecta Corp. is recalling BD Nano 2nd Gen Pen Needles that were distributed at or after their February 29, 2024 expiration date. Using expired needles cannot guarantee sterility and integrity.
Product
BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count sample contained in Patient Counseling Sample Toolbox -Catalog 6484755/Lot Number: 3750144)-Sterile, single use devices designed for the parenteral administration of a drug from a cartridge contained in a drug pen injector…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2430-2024·2024-07-31
Abbott Infinity 5 Pulse Generator May Fail Prematurely
Abbott is recalling 5,900 Infinity 5 implantable pulse generators because the replacement indicator and end-of-service date may be shorter than labeled, potentially causing premature device failure. Patients should contact their doctor about device status.
Product
Abbott Infinity 5, Implantable Pulse Generator, REF: 6661, SterileEO, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1516-2024·2024-07-31
Indigenous Collection Signature Plates recalled for potential lead contamination
Canadian Art Prints is recalling Indigenous Collection Signature Plates sets due to potential leachable lead exceeding FDA guidance levels. The affected sets were distributed across 18 US states.
Product
UPC 772665860106. PLT010. Indigenous Collection Signature Plates set - Dancing Bears & Three Bears on box and back of plate. Art by Dawn Oman. Brand Indigenous Collection by CAP on box and back of plate. The Dancing Bears is a scene with three dancing polar bears with a night…
Category
Consumer Product
Distribution
18 states
HighFDA (Devices)·Z-2431-2024·2024-07-31
Abbott Infinity 7 Pulse Generator May Have Shorter-Than-Labeled Service Date
The Abbott Infinity 7 implantable pulse generator's replacement indicator and end-of-service date may be shorter than the product labeling states, potentially leading to loss of therapy for patients.
Product
Abbott Infinity 7, Implantable Pulse Generator, REF: 6662, SterileEO, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1515-2024·2024-07-31
Glazed ceramic plates recalled for exceeding lead guidance levels
Canadian Art Prints is recalling Indigenous Collection Signature Plates sets because the glazed ceramic plates may exceed FDA guidance levels for leachable lead. Consumers should stop using these plates immediately.
Product
UPC Code 772665860083, Stock code PLT008, Indigenous Collection Signature Plates set - Not Forgotten & Ancient Messages. Artist Maxine Noel on box and back of plates. Brand Indigenous Collection by CAP on box and back of plates. Not Forgotten is an image of a woman with…
Category
Consumer Product
Distribution
18 states
ModerateFDA (Food)·F-1492-2024·2024-07-31
Dried Plums Recalled for Undeclared Cyclamate Content
Sweet Preserved Dried Plums from Farmer's Grange contain undeclared cyclamate sweetener. The product was distributed in select U.S. states and should not be consumed.
Product
Sweet Preserved Dried Plums; Farmer's Grange; Series Food; 88g; Plastic synthetic (flexible) package; INGREDIENTS: Plum, Salt, Sugar, ADDITIVES: Clove, Cinnamon, Liquorice, Citric acid, Red #40.; Product contains sulfite; PRODUCT OF CHINA (T.F.C).
Category
Food
Distribution
5 states
ModerateFDA (Drugs)·D-0616-2024·2024-07-31
Hemp Bombs CBD Pain Freeze Recalled for Subpotent Menthol Content
Hemp Bombs CBD Pain Freeze is being recalled because the menthol content is weaker than the labeled 4% claim. The recall affects 2,082 bottles distributed nationwide.
Product
Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC Code: 8-40078-56612-7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0615-2024·2024-07-31
Hemp Bombs CBD Pain Freeze Recalled Due to Subpotent Menthol Content
Global Widget LLC is recalling Hemp Bombs CBD Pain Freeze (4% menthol) because the menthol concentration is below the labeled claim. Approximately 11,130 bottles were distributed nationwide.
Product
Hemp Bombs CBD Pain Freeze (menthol 4%), 400mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC code: 8-40078-56497-0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2425-2024·2024-07-31
Cystatin C Diagnostic Reagent Marketed Without FDA 510(k) Clearance
Randox Laboratories is recalling 115 kits of RX Series CYSC Cystatin C Reagent because it was marketed without required FDA 510(k) clearance. Healthcare facilities should discontinue use and contact the manufacturer.
Product
RX Series CYSC- Cystatin C Reagent -Intended for in vitro diagnostic (IVD) use as Randox Cystatin C assay on automated analysers. Catalogue Number: CYS4004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2422-2024·2024-07-31
MIC-KEY Gastric-Jejunal Feeding Tube Kits Recalled for Incomplete Safety Information
Avanos Medical is recalling MIC-KEY Gastric-Jejunal Feeding Tube Kits because the Instructions for Use were missing required risk information about potential complications. No illnesses have been reported.
Product
MIC-KEY* Gastric-Jejunal Feeding Tube Kit, Endoscopic / Radiologic Placement, Low-Profile GJ-Tube, REF 0270xx (Non-ENFIT); and MIC-KEY* Gastric-Jejunal Feeding Tube Kit, Extension Sets with ENFit Connectors, Endoscopic / Radiologic Placement, Low-Profile GJ-Tube, REF 8270xx…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0613-2024·2024-07-31
Hemp Bombs CBD Pain Freeze Recalled Due to Subpotent Menthol Content
Hemp Bombs CBD Pain Freeze is being recalled because the menthol potency is less than the labeled 4%. Consumers should stop using the affected product and return it to the retailer.
Product
Hemp Bombs CBD Pain Freeze (menthol 4%), 100mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, NDC 73423-003-01; UPC Code: 8-40078-56493-2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2439-2024·2024-07-31
Medical device diagnostic software vulnerability causes potential application crashes
Siemens Sensis Vibe diagnostic systems may crash when documentation functionality is used during certain reporting events. Seven units were distributed to facilities nationwide.
Product
Sensis Vibe systems with software version VD15B in combination with VM VIRTUAL SERVER Model: 10765502-Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0614-2024·2024-07-31
Nature's Script CBD Pain Relief Roll-On Recalled for Subpotent Menthol
FDA Class III recall of Nature's Script CBD Cryotherapy Pain Relief Roll-on (200mg, 1 oz bottles) due to subpotent menthol content less than the labeled 4%. The product did not contain the claimed amount of active ingredient.
Product
Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, UPC code: 8-40078-56731-5
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0618-2024·2024-07-31
Homeopathic Kit Recalled for Label Mix-up Between Products
Washington Homeopathic Products is recalling 11 Complete 30C/200C Homeopathic Kits nationwide due to a labeling error. Some bottles labeled as Ferrum Metallicum 200C actually contain Ferrum Phosphoricum 200C.
Product
Complete 30C/200C Homeopathic Kit, Contains: One hundred 1/2 dram vials of homeopathic medicines, Washington Homeopathic Products, Inc., Berkley Springs, WV 25411, UPC 7 40640 64300 6.
Category
Drug
Distribution
Distributed nationwide
CriticalUSDA FSIS·023-2024-EXP·2024-07-30
Boar's Head Expands Recall of Deli Meats Due to Listeria
Boar's Head is recalling 7 million pounds of ready-to-eat meat and poultry products due to possible Listeria contamination linked to a multistate outbreak.
Product
Boar's Head Provisions Co., Inc. — Boar's Head Provisions Co. Expands Recall for Ready-To-Eat Meat and Poultry Products Due to Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·24V566000·2024-07-30
Tiffin motorhome chassis controller can blow a fuse shutting down engine
Tiffin is recalling certain 2022-2025 Phaeton, Allegro Bus and Zephyr motorhomes because the PowerGlide chassis controller may have insufficient circuit protection, which can blow a fuse and shut down the engine.
Product
TIFFIN — TIFFIN ALLEGRO BUS, PHAETON, ZEPHYR
Category
Vehicle
Distribution
Distributed nationwide