# FDA recall Z-1183-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2025-01-09.

## Product

Medline Convenience Kits for Various Procedures:  1) CLOVIS RESP/INTUB DRAWER 2, Model Number ACC010809;  2) RESP/INTUBATION DRAWER #2, Model Number ACC010813

## Reason for recall

Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.

## Distribution

US States: CA, NY

## Key facts

- **Recall number:** Z-1183-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-09
- **Report date:** 2025-02-26

- **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-1183-2025

## Citation

> AI Analytics. FDA recall Z-1183-2025. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1183-2025. Source: US FDA. Licensed CC0.

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