Sklar Instruments: Device Recall

Recall #Z-0929-2025 · 12/03/2024

Class II: Risk

Recall Details

Recall Number
Z-0929-2025
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
75 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 WEITLANER RETR SH 2X3 4.5"CS25, Model Numbers: 96-2201A; 2) ECONO STERILE WEITLANER RETR BL 2X3 4.5"CS25, Model Numbers: 96-2203A; 3) ECONO STERILE WEITLANER RETR BL 3X4 5.5"CS25, Model Numbers: 96-2207A; 4) ECONO STERILE WEITLANER RETR SH 3X4 5.5"CS25, Model Numbers: 96-2208A; 5) ECONO STERILE WEITLANER RETR 3X4 SH 8" CS/10, Model Numbers: 96-2209A; 6) ECONO STERILE WEITLANER RETR 3X4 BL 8" CS/10 , Model Numbers: 96-2210A; 7) ECONO STERILE HOLZHEIMER RETR 4PRG SH 4"CS25, Model Numbers: 96-2241A; 8) ECONO STERILE HOLZHEIMER RETR 4PRG BL 4"CS25, Model Numbers: 96-2242A; surgical retractor

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.