Sklar Instruments: Device Recall

Recall #Z-0944-2025 · 12/03/2024

Class II: Risk

Recall Details

Recall Number
Z-0944-2025
Classification
Class II
Product Type
Device
Recalling Firm
Sklar Instruments
Status
Ongoing
Date Initiated
12/03/2024
Location
West Chester, PA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
475 units

Reason for Recall

Reports of various packaging issues that may result in a breach of the sterile barrier.

Product Description

ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE GRAVES SPEC STRL SM BX/25, Model Number 96-2603; 2) ECONO STERILE GRAVES SPEC STRL MD BX/25, Model Number 96-2605; 3) ECONO STERILE GRAVES SPEC STRL LG BX/25, Model Number 96-2607; 4) ECONO STERILE PEDERSON SPEC STERILE" SM BX/25, Model Number 96-2613; 5)ECONO STERILE PEDERSON SPEC STRL MD BX/25, Model Number 96-2615; 6) ECONO STERILE PEDERSON SPEC STRL LG BX/50, Model Number 96-2616; 7) ECONO STERILE PEDERSON SPEC STRL LG BX/25, Model Number 96-2617; 8) ECONO STERILE GRAVES VAG SPEC STRL MD CS/50, Model Number 96-3001; 9) ECONO STERILE GRAVES VAG SPEC STRL LG CS/50, Model Number 96-3002; speculum, gynecological

Distribution Pattern

Domestic: Nationwide Distribution

Other Recalls by Sklar Instruments

View all recalls by Sklar Instruments →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.