# FDA recall Z-0640-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-10-09.

## Product

MEDLINE convenience kits labeled as:    1) BASIC NEURO PACK, REF CDS780202P;   2) BASIC NEURO PACK, REF CDS780202Q;   3) BASIC NEURO PACK, REF CDS780202R;   4) ACDF CDS, REF CDS941061M;   5) NEURO KIT, REF CDS981327Q;   6) ZALE V-P SHUNT CDS, REF CDS983186J;   7) NEURO PACK-LF, REF DYNJ0038440C;   8) NEURO PACK-LF, REF DYNJ0406347M;   9) NEURO-LF, REF DYNJ0484186M;   10) NEURO-LF, REF DYNJ0484186N;   11) NEURO VP SHUNT PACK-LF, REF DYNJ0843121K;   12) NEURO VP SHUNT/VAGAL NERVE-RF, REF DYNJ21925S;   13) NEURO-ORTHO EXTRAS, REF DYNJ44882L;   14) NEURO PACK, REF DYNJ57785B;   15) NEURO PACK, REF DYNJ60825B;   16) CHRISTUS MC NEURO PACK, REF DYNJ61157C;   17) CHRISTUS CHILDRENS NEURO PK, REF DYNJ61168C;   18) CHRISTUS CHILDRENS VP SHUNT PK, REF DYNJ61174C;   19) AFCH SHUNT, REF DYNJ63317C;   20) NEURO SPINE PK, REF DYNJ63319D;   21) NEURO CAROTID ENDARTERECTO, REF DYNJ63321D;   22) DBS PACK, REF DYNJ63322A;   23) NEURO LAM, REF DYNJ64188B;   24) PACK,V-P SHUNT, REF DYNJ65472B;   25) NEURO

## Reason for recall

Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0640-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-09
- **Report date:** 2024-12-11

- **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-0640-2025

## Citation

> AI Analytics. FDA recall Z-0640-2025. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-0640-2025. Source: US FDA. Licensed CC0.

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