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

Recall Z-0943-2025 — ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE SIMS UTERINE CURETTE #3 STER25, Model Number 96-4113; 2) ECONO STERILE KEVORK ENDO CURET W/BAS STER25, Model Number 96-4144A; 3) ECONO STERILE KEVORKIAN CURET W/O BAS STER25, Model Number 96-4145A; cervical biopsy

U.S. FDA — Device Enforcement · United States · 2024-12-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0943-2025
Date of alert
2024-12-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Sklar Instruments
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
50649111492899
Reported risk: Reports of various packaging issues that may result in a breach of the sterile barrier.
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.

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