# FDA recall Z-2747-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-04-08.

## Product

Medline procedural kits labeled as:    1) TYMPANOPLASTY , Pack Number CDS980203S;   2) MAJOR EAR , Pack Number CDS982016T;   3) MAJOR EAR PACK, Pack Number CMPJ01846O;   4) EAR PACK, Pack Number CMPJ05884J;   5) MZ EAR PACK , Pack Number CMPJ09860D;   6) KIT MAJOR EAR CHRG, Pack Number CMPJ09914C;   7) ENT PACK, Pack Number CMPJ13389A;   8) ENT PACK, Pack Number CMPJ13389B;   9) ENT PACK, Pack Number CMPJ13389C;   10) DR LIN EAR PACK , Pack Number CMPJ13509 ;   11) TYMPANOPLASTY PACK, Pack Number CMPJ21114O;   12) EAR PACK-LF , Pack Number DYNJ0425965G  ;   13) EAR PACK-LF , Pack Number DYNJ0774664K  ;   14) HL EAR PACK , Pack Number DYNJ40560B;   15) HL EAR PACK , Pack Number DYNJ40560BH;   16) EAR PACK, Pack Number DYNJ44134C;   17) EAR PACK, Pack Number DYNJ44134D;   18) EAR PACK, Pack Number DYNJ44134F;   19) MINOR ENT PACK, Pack Number DYNJ45577A;   20) ENT PACK, Pack Number DYNJ48595 ;   21) MH NASAL, Pack Number DYNJ49888I;   22) MH NASAL, Pack Number DYNJ49888J;   23) MIDDLE EA

## Reason for recall

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

## Distribution

Worldwide

## Key facts

- **Recall number:** Z-2747-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-08
- **Report date:** 2024-09-04

- **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-2747-2024

## Citation

> AI Analytics. FDA recall Z-2747-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2747-2024. Source: US FDA. Licensed CC0.

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