Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2167-2024 — CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical procedures where fragmentation, emulsification and aspiration of soft and hard tissue Catalog Number: C2600* *Note: you may see C2600P or C2600SRL on labeling. This notice is applicable for those SKUs as well

U.S. FDA — Device Enforcement · United States · 2024-05-29 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2167-2024
Date of alert: 2024-05-29
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Integra LifeSciences Corp.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10381780039419

Reported risk: Potential for the CUSA Excel 23KHz Straight Handpiece housing to crack, may result in delay of treatment

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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