# FDA recall Z-0634-2025

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

## Product

MEDLINE convenience kits labeled as:    1) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907I;   2) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907K;   3) LKLND SNGL BASIN PK RFID-LF, REF DYNJ0619907L;   4) BASIN SET W/ RING BASIN, REF DYNJ06966M;   5) OPEN HEART C--BASIN PACK-LF, REF DYNJ0867331G;   6) TOTAL KNEE BASIN B PACK-LF, REF DYNJ0867555L;   7) ST. ANNE'S MINOR BASIN PACK, REF DYNJ24622K;   8) ST. ANNE'S MAJOR BASIN SET UP, REF DYNJ24628M;   9) MAJOR BASIN SET, REF DYNJ41285B;   10) BASIN PACK, REF DYNJ50123D;   11) MAJOR BASIN TRAY, REF DYNJ54461F;   12) MAJOR BASIN TRAY, REF DYNJ54461G;   13) MAJOR BASIN TRAY, REF DYNJ54461I;   14) TR-MINOR KIT-LF, REF DYNJ54801F;   15) TR-MAJOR KIT-LF, REF DYNJ54802I;   16) MAJOR BASIN PACK, REF DYNJ59816A;   17) SINGLE BASIN PACK ST VINCENT, REF DYNJ60529D;   18) BASIN PACK, REF DYNJ60812B;   19) BASIN PACK SH, REF DYNJ60812C;   20) PLASTIC BASIN PACK, REF DYNJ63883C;   21) MINOR PACK, REF DYNJ63961D;   22) OSC BREAST PACK, REF DYNJ65808B;   2

## 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-0634-2025
- **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-0634-2025

## Citation

> AI Analytics. FDA recall Z-0634-2025. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-0634-2025. Source: US FDA. Licensed CC0.

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