# FDA recall Z-2987-2024

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

## Product

Medline Convenience kits, labeled as:   1) SINGLE SHOT EPIDURAL PACK-LF, Pack Number DYNJ0708470K ;  2) EPIDURAL CSTM PACK-LF , Pack Number DYNJ0844004;  3) CUSTOM EPIDURAL PACK-LF , Pack Number DYNJ0934752F ;  4) EPIDURAL PACK-LF, Pack Number DYNJ0957053D ;  5) EPIDURAL PACK-LF, Pack Number DYNJ0957053DH;  6) SINGLE SHOT TRAY, Pack Number DYNJ32736;  7) CONTINUOUS EPIDURAL TRAY-LF , Pack Number DYNJ34352A ;  8) SINGLE SHOT EPIDURAL-LF , Pack Number DYNJ36046A ;  9) PHOENIXVILLE EPIDURAL TRAY, Pack Number DYNJ40991A ;  10) UNIVERSAL SCOPE PACK, Pack Number DYNJ45052A ;  11) SPINAL PACK , Pack Number DYNJ48916B ;  12) PUH SPINAL BLOCK TRAY , Pack Number DYNJ49205B ;  13) EPIDURAL PACK , Pack Number DYNJ50772A ;  14) TRANSFORAMINAL PACK , Pack Number DYNJC3420D ;  15) EPIDURAL PREP TRAY-LF , Pack Number DYNJRA0135B;  16) SUPPORT TRAY-LF, Pack Number DYNJRA0198;  17) SPINAL TRAY W/GERTIE MARX NDL , Pack Number DYNJRA0245 ;  18) EPIDURAL TRAY , Pack Number DYNJRA0260 ;  19) SPINAL EPIDURAL

## 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-2987-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-08
- **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-2987-2024

## Citation

> AI Analytics. FDA recall Z-2987-2024. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-2987-2024. Source: US FDA. Licensed CC0.

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