# FDA recall Z-0724-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-11-06.

## Product

Medline brand, medical procedure convenience kits, labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, SKU CDS780119T;   2) NEURO KIT, SKU CDS981327Q;   3) NEURO POSTERIOR SPINE PACK-LF, SKU DYNJ0311501I;   4) ACOUSTIC NEUROMA PACK-LF, SKU DYNJ37741D;   5) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836C;   6) SCRIPPS SW NEURO PACK-LF, SKU DYNJ39836D;   7) NEURO BUNDLE-LF, SKU DYNJ40095A;   8) NEURO BUNDLE-LF, SKU DYNJ40095B;   9) NEURO BUNDLE-LF, SKU DYNJ40095C;   10) NEURO BUNDLE-LF, SKU DYNJ40095D;   11) NEURO PACK-LF, SKU DYNJ42844D;   12) WMC VP SHUNT PACK-LF, SKU DYNJ50629J;   13) NEURO PACK, SKU DYNJ54255A;   14) NEURO CHRISTUS, SKU DYNJ61190A;   15) NEURO KIT, SKU DYNJ62854B;   16) NEURO KIT, SKU DYNJ62854C;   17) NEURO PACK NTX, SKU DYNJ66213D;   18) NEURO PACK, SKU DYNJ67628C;   19) BASIC NEURO CUSTOM, SKU DYNJ83387;   20) BASIC NEURO CUSTOM, SKU DYNJ83387A;   21) HALY NEURO PACK, SKU DYNJ87308;   22) FHWC NEURO, SKU DYNJ906131B;   23) CRANI, SKU DYNJ907865;   24) KIT NEURO LAFAYETTE, SKU DY

## Reason for recall

Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods

## Distribution

US Nationwide. Canada.

## Key facts

- **Recall number:** Z-0724-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-11-06
- **Report date:** 2025-01-01

- **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-0724-2025

## Citation

> AI Analytics. FDA recall Z-0724-2025. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-0724-2025. Source: US FDA. Licensed CC0.

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