# FDA recall Z-2703-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-03-22.

## Product

Medline medical procedure kits labeled as follows:      a) BASIC NASAL, REF DYNJ909932;   b) BRONCH KIT, REF DYKE1007B;   c) ENT, REF DYNJ909935;   d) NASAL SINUS-LF, REF DYNJ902624G;   e) ORAL, REF DYNJ902377I;   f) PACK,BRONCHOSCOPY, REF DYNJ65475B;   g) PACK,HEAD AND NECK, REF DYNJ65487B;   h) PACK,SINUS, REF DYNJ906898;   i) PACK,T & A, REF DYNJ906897B;   j) PACK,T & A ASC, REF DYNJ906914;   k) T AND A, REF DYNJ909941

## Reason for recall

A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.

## Distribution

Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.

## Key facts

- **Recall number:** Z-2703-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-22
- **Report date:** 2024-08-28

- **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-2703-2024

## Citation

> AI Analytics. FDA recall Z-2703-2024. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-2703-2024. Source: US FDA. Licensed CC0.

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