# FDA recall Z-0929-2025

> **Sklar Instruments** · Class II · device recall initiated 2024-12-03.

## Product

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

## Reason for recall

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

## Distribution

Domestic: Nationwide Distribution

## Key facts

- **Recall number:** Z-0929-2025
- **Recalling firm:** Sklar Instruments
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-12-03
- **Report date:** 2025-01-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** West Chester, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0929-2025

## Citation

> AI Analytics. FDA recall Z-0929-2025. Retrieved 2026-07-29 from https://api.ai-analytics.org/recall/Z-0929-2025. Source: US FDA. Licensed CC0.

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