# FDA recall Z-2635-2024

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

## Product

Medline Convenience kits, labeled as:   1) NERVE STIMULATOR, Pack Number CDS981579O ;  2) DR DIULUS INJECTION PACK, Pack Number DYNDA2391;  3) BLOCK KIT , Pack Number DYNDA2508;  4) NERVE BLOCK PAIN PACK, Pack Number DYNDL1389;  5) BLOCK TRAY-LF , Pack Number DYNJ0117039;  6) NERVE BLOCK ACCESSORY PACK, Pack Number DYNJ0134147D ;  7) UNIVERSAL PROC TRAY-LF, Pack Number DYNJ02120B ;  8) ANGIO PROCEDURE PACK-LF , Pack Number DYNJ0298504AJ;  9) CUSTOM BLOCK KEMP PACK-LF , Pack Number DYNJ0371999G ;  10) PAIN MANAGEMENT PACK-LF , Pack Number DYNJ0374104F ;  11) THORASCOPIC - UNIV, Pack Number DYNJ0375880O ;  12) ANGIOGRAPHIC PACK II-LF , Pack Number DYNJ0543507AB;  13) GM ANGIOGRAPHY PACK-LF, Pack Number DYNJ0621584Y ;  14) ANGIOGRAPHY PACK-LF , Pack Number DYNJ0689247S ;  15) PERI NEURO BLOCK PACK-LF, Pack Number DYNJ0703127A ;  16) MAJOR HEAD/NECK PACK-LF , Pack Number DYNJ0826705L ;  17) STANDARD BLOCK PACK-LF, Pack Number DYNJ0957047C ;  18) STANDARD BLOCK PACK-LF, Pack Number DYNJ0957

## 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 distribution.

## Key facts

- **Recall number:** Z-2635-2024
- **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-2635-2024

## Citation

> AI Analytics. FDA recall Z-2635-2024. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-2635-2024. Source: US FDA. Licensed CC0.

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