# FDA recall Z-0475-2026

> **Medline Industries, LP** · Class II · device recall initiated 2025-10-01.

## Product

Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated, Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

## Reason for recall

Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0475-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-01
- **Report date:** 2025-11-19

- **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-0475-2026

## Citation

> AI Analytics. FDA recall Z-0475-2026. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0475-2026. Source: US FDA. Licensed CC0.

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