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Lower risk Medical device recall · FDA · Published July 24, 2024

Stryker iBur 3.0mm Coarse Diamond Round Recall: Risk of Thermal Injury During Bone Surgery

Stryker recalls certain iBur 3.0mm Coarse Diamond Round surgical burs for potential thermal injury during bone procedures. Affected units may cause minor tissue damage requiring medical attention.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2727-2024Medical deviceStryker ›
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Contact the company

Recalling firmStryker Corporation1941 Stryker Way · Portage, MI 49002-9711
✎ GovInfoNow plain-language explainer

Stryker is recalling specific surgical burs that could overheat during bone cutting procedures, potentially causing minor tissue damage or requiring medical intervention. This recall affects surgeons and medical professionals using the product for spinal, neuro, ENT, and endoscopic surgeries. Read more at govinfonow.com/recall/54555-stryker-ibur-3-0mm-coarse-diamond-round-recall-risk-of.

Source Summary by GovInfoNow · govinfonow.com/recall/54555-stryker-ibur-3-0mm-coarse-diamond-round-recall-risk-of · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2727-2024

Cite this page

“Stryker iBur 3.0mm Coarse Diamond Round Recall: Risk of Thermal Injury During Bone Surgery.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54555-stryker-ibur-3-0mm-coarse-diamond-round-recall-risk-of. Based on FDA recall #Z-2727-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2727-2024%22&limit=1).

The FDA announced on July 24, 2024, that Stryker Corporation is recalling Stryker iBur 3.0mm Coarse Diamond Round, Distal Bend surgical burs due to potential thermal injury risks. The agency classified the recall as Class II.

How to tell if you have it

  • Stryker iBur 3.0mm Coarse Diamond Round, Distal Bend
  • UPC: 07613327501209
  • Lot Numbers: 22230017, 22333017, 22342017, 23011017, 23093017, 23172017, 23188017, 23221017, 23311017, 24004027

The hazard

The product may exhibit temperatures higher than specification where the bur shank meets the distal bushing. Temperatures higher than specification may lead to the potential for minor tissue/structure damage or tissue/structure damage from thermal injury which may need medical/surgical intervention.

Context

GovInfoNow's records show Stryker Corporation has 34 other recalls on record since November 17, 2017. Other recent recalls of similar products include Stryker Single Spike Tube Set Leaks During Use (June 8, 2026), Stryker Neptune Smart Docking Station Recall: Electrical Shock Risk (May 6, 2026), and Stryker FluidSmart Urology Tube Set Recall: Nonconforming Products Distributed (April 9, 2026). Other recent recalls of similar products include I.T.S. Distal Humeral Plates Risk MRI Heating (January 23, 2026), I.T.S. LRS Orthopedic Plates: MRI Safety Risk from Temperature Increases (January 23, 2026), and Surgify Halo 40mm Drill Risk: Burr Breakage During Spinal Surgery (April 30, 2026).

How to tell if you have this one

Check for the product model 'Stryker iBur 3.0mm Coarse Diamond Round, Distal Bend' with lot numbers 22230017, 22333017, 22342017, 23011017, 23093017, 23172017, 23188017, 23221017, 23311017, or 24004027.

  • Brand
    Stryker
  • Product
    Stryker iBur 3.0mm Coarse Diamond Round, Distal Bend
  • Category
    Medical device
FDA recall event · 10 products

All 10 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Completed
  • Distribution
    Worldwide distribution - US Nationwide and the countries of Australia, Canada, France, Hong Kong, India, Italy, Japan, Japan, Netherlands, South Korea, Spain, Sweden, Taiwan, United Kingdom.
Recall numberProduct, codes & lotsQuantity
Z-2722-2024Stryker iBur 3.0mm Precision Round, Distal Bend- Intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-009-030; GTIN: 07613327501247 Lot Numbers: 22224017 22234017 22234027 22250017 22293017 22299017 23157017 23179017 23179027 232990171612 units
Z-2723-2024Stryker iBur 4.0mm Precision Round, Distal Bend- intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-009-040; GTIN: 07613327501223 Lot Numbers: 22245017 22248017 22270017 22299017 22306027 231880171227 units
Z-2724-2024Stryker iBur 2.0mm Diamond Round, Distal Bend- intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-012-020D; GTIN: 07613327501261 Lot Numbers: 22237017 22241017 22334017 23085017 23179017 23213017 24003017 240150171226 units
Z-2725-2024Stryker iBur 3.0mm Diamond Round, Distal Bend - intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-012-030D; GTIN: 7613327501230 Lot Numbers: 22216017 22230017 22334017 23004017 23004027 23009017 23157017 23208017 23233017 23233027 240030172507 units
Z-2726-2024Stryker iBur 4.0mm Diamond Round, Distal Bend- intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-012-040D; GTIN: 07613327501278 Lot Numbers: 22334017 22339017 23004017 23016017 23085017 23115017 23195017 232990171706 units
Z-2727-2024Stryker iBur 3.0mm Coarse Diamond Round, Distal Bend - intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-013-030DC; GTIN: 07613327501209 Lot Numbers: 22230017 22333017 22342017 23011017 23093017 23172017 23188017 23221017 23311017 240040272670 units
Z-2728-2024Stryker iBur 4.0mm Coarse Diamond Round, Distal Bend - intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-013-040DC; GTIN: 07613327501155 Lot Numbers: 22248017 22263017 22334017 22348017 22348027 23016027 23095027 23128017 23163017 23179017 23205017 23205027 23205037 23221017 23311017 24004017 24004027 240040375031 units
Z-2729-2024Stryker iBur 5.0mm Coarse Diamond Round, Distal Bend intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-013-050DC; GTIN: 07613327501186 Lot Numbers: 22224017 22227017 23087017 23157017 23188017 233420171171 units
Z-2730-2024Stryker iBur 3.0mm Diamond Match Head, Distal Bend - intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-107-030D; GTIN: 07613327509229 Lot Numbers: 22334017 23047017 23095017 231980172507 units
Z-2731-2024Stryker iBur 3.0mm Precision Match Head, Distal Bend- intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-107-530; GTIN: 07613327501193 Lot Numbers: 22228017 22257017 22269017 22276017 23085017 23095017 23157017 23157027 23179017 23179027 23198017 23213017 23221017 23299017 23345017 233450273673 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the lot number on the product label to confirm if it's affected.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide distribution - US Nationwide and the countries of Australia, Canada, France, Hong Kong, India, Italy, Japan, Japan, Netherlands, South Korea, Spain, Sweden, Taiwan, United Kingdom.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 42 days after the firm started it.

1. Firm started the recall: Jul 24, 202412. FDA classified it Class II: Aug 26, 202423. Published in FDA’s Enforcement Report: Sep 4, 202432024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-2727-2024 (July 24, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2727-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA