# FDA recall Z-0783-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-11-21.

## Product

Medline custom medical procedure kits labeled as:    1) FREE FLAP BASIC SET-UP PK, REF DYNJ0991320J;   2) MVFF/FIBU #54-RF, REF DYNJ21927R;   3) FUNCTIONAL SINUS ENDOSCOPY, REF DYNJ40406A;   4) DR GOLDSTEIN ACCESSORY PACK, REF DYNJ51818F;   5) ENDOSCOPIC SKULL BASE, REF DYNJ58648F;   6) DIEP FLAP, REF DYNJ66867A;   7) KIT FREE FLAP MOSES, REF DYNJ905366A;   8) FREE FLAP, REF DYNJ905634B;   9) ROBOTIC THORACIC, REF DYNJ907817;   10) TRANSPHENOIDAL, REF DYNJ908165;   11) METREX, REF DYNJ910072;   12) DIEP FLAP, REF DYNJ910120A.

## Reason for recall

Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.

## Distribution

Worldwide distribution - US Nationwide and the countries of UAE, and Canada.

## Key facts

- **Recall number:** Z-0783-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-11-21
- **Report date:** 2025-01-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0783-2025

## Citation

> AI Analytics. FDA recall Z-0783-2025. Retrieved 2026-09-22 from https://api.ai-analytics.org/recall/Z-0783-2025. Source: US FDA. Licensed CC0.

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