# FDA recall Z-0779-2025

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

## Product

Medline custom medical procedure kits labeled as:    1) VP SHUNT CDS, REF CDS983470D;   2) 1/2X1/2 NEURO SPONGE PACK-LF, REF DYNJ0713177;   3) BURR HOLE SHUNT PACK, REF DYNJ56819D;   4) BURR HOLE SHUNT PACK, REF DYNJ56819F;   5) BURR HOLE SHUNT PACK, REF DYNJ56819G;   6) RO VP SHUNT PACK, REF PHS392834010D;   7) VP SHUNT, REF SYNJ10307A.

## 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-0779-2025
- **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-0779-2025

## Citation

> AI Analytics. FDA recall Z-0779-2025. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-0779-2025. Source: US FDA. Licensed CC0.

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