# FDA recall Z-3114-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-06-27.

## Product

Medline convenience kits containing semi-rigid suction liners labeled as follows:  a)  ENDO KIT, Pack Number DYKE1092B;   b) VIDEO BRONCHOSCOPY TRAY, Pack Number DYKE1666;   c) SUCTION CANISTER KIT, Pack Number DYKM2196;   d) SUCTION CANISTER KIT, Pack Number DYKM2196H;   e) BRONCH LAB PACK-LF, Pack Number DYNJ24810B;   f) THORACIC, Pack Number DYNJ907991F;   g) RECTAL, Pack Number DYNJ908108A;   h) ROBOTIC, Pack Number DYNJ908109C;   i) CERVICAL, Pack Number DYNJ908748D;   j) LAMI, Pack Number DYNJ908750D;   k) MERCY TIFFIN BASIC-LF, Pack Number DYNJ909731;   l) MERCY TIFFIN LITHOTOMY, Pack Number DYNJ909735;   m) BASIC GENERAL SET UP, Pack Number DYNJ909945;   n) BASIC GENERAL SET UP, Pack Number DYNJ909945A;   o) AMB OCULOPLASTICS MUSC, Pack Number DYNJ910289;   p) AMB OCULOPLASTICS MUSC, Pack Number DYNJ910289H;   q) MTHZ TOTAL HIP, Pack Number DYNJC9311M;   r) BRONCH KIT, Pack Number P906877

## Reason for recall

Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Panama.

## Key facts

- **Recall number:** Z-3114-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-27
- **Report date:** 2024-09-18

- **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-3114-2024

## Citation

> AI Analytics. FDA recall Z-3114-2024. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-3114-2024. Source: US FDA. Licensed CC0.

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