Integra recalls CUSA Excel 23KHz handpieces made before Nov 2023 due to potential housing cracks causing treatment delays. Affected units have specific serial numbers and manufacturing dates.
“Integra CUSA Excel 23KHz Handpiece Recall: Housing Crack Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54992-integra-cusa-excel-23khz-handpiece-recall-housing-crack-risk. Based on FDA recall #Z-2167-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2167-2024%22&limit=1).
Integra LifeSciences Corp. voluntarily recalled CUSA Excel C2600 23KHz Straight Handpieces on May 29, 2024, according to the FDA. The housing may crack, potentially delaying treatment. Owners should contact the company for a replacement.
Catalog Number: C2600 (includes C2600P and C2600SRL SKUs)
UDI-DI: 10381780039419
Serial Numbers: Manufactured prior to HAL23XXXXXXIE
Manufacture Date: Prior to 11/01/2023
The hazard
The CUSA Excel 23KHz Straight Handpiece housing has the potential to crack, which may result in a delay of treatment.
Context
GovInfoNow's records show Integra LifeSciences Corp. has had 35 other recalls on record since 2017-08-18. Other recent recalls include the Integra AURORA Surgiscope System Recall (2025-02-06), the MediHoney Wound Dressing Gel Recall (2025-01-10), and the Integra LifeSciences CODMAN CERTAS Plus Valve Recall (2024-12-16). Other recent recalls of similar products include the Acumed Hexalob Screw Recall (2026-05-28), the Stryker XCEL Bladeless Trocar W/Stability Sleeve 12x100mm Recall (2026-08-19), and the Stryker Hoffmann II Connecting Rod Micro 3 x 50mm recall (2026-07-01).
How to tell if you have this one
Check for serial numbers starting with 'HA' followed by two digits (e.g., HAL23XXXXXXIE) indicating November 2023 manufacture. Units made before November 2023 are affected.
Brand
Integra
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Serial Number
Look for serial numbers starting with 'HA' followed by two digits indicating the month and year of manufacture.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Nationwide Foreign: Argentina Australia Bangladesh Bangladesh Belgium Bolivia (Plurinational State of) Brazil Canada Chile China Costa Rica Dominican Republic (the) El Salvador Hong Kong India Indonesia Japan Korea (the Republic of)…” 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 35 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-2167-2024 (May 29, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2167-2024 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.