# FDA recall Z-0630-2025

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

## Product

MEDLINE convenience kits labeled as:   2) ABDOMINAL LAPAROSCOPY, REF CDS760057K;  3) ABDOMINAL LAPAROSCOPY, REF CDS760057L;  4) MAJOR LAPAROTOMY CDS, REF CDS860015W;  5) MINOR LAPAROTOMY CDS, REF CDS860016P;  6) MINOR LAPAROTOMY CDS, REF CDS860016Q;  7) MINOR LAPAROTOMY CDS, REF CDS860016R;  8) LAPAROTOMY CDS #31-RF, REF CDS860062R;  9) LAPAROTOMY CDS #31-RF, REF CDS860062S;  10) LAPAROSCOPY CDS, REF CDS860194I;  11) BASIC LAPAROSCOPY CDS, REF CDS920080R;  12) BASIC LAPAROSCOPY CDS, REF CDS920080S;  13) BASIC LAPAROSCOPY CDS, REF CDS920080T;  14) GENERAL LAPAROSCOPY, REF CDS930027U;  15) GENERAL LAPAROSCOPY, REF CDS930027V;  16) MINOR BASIC-LF, REF CDS930120G;  17) MINOR BASIC-LF, REF CDS930120I;  18) MAJOR DRAPE-LF, REF CDS930121L;  19) GENERAL LAPAROSCOPY PROCEDURE, REF CDS930125U;  20) GENERAL MINOR CDS, REF CDS980246V;  21) MAJOR PROCEDURE-LF, REF CDS980255T;  22) MAJOR LAPAROTOMY, REF CDS981133K;  23) MAJOR LAPAROTOMY KIT, REF CDS981316T;  24) MINOR KIT, REF CDS981317V;  25) BAPTI

## 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-0630-2025
- **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-0630-2025

## Citation

> AI Analytics. FDA recall Z-0630-2025. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-0630-2025. Source: US FDA. Licensed CC0.

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