# FDA recall Z-2634-2024

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

## Product

Medline convenience kits, labeled as:  1) PAIN SERVICES CDS , Pack Number CDS985445B ;  2) PAIN SERVICES CDS , Pack Number CDS985445C ;  3) PAIN TRAY , Pack Number DYNDA1233B ;  4) PAIN TRAY , Pack Number DYNDA2402A ;  5) C ARM BLOCK PACK, Pack Number DYNDA2795;  6) SINGLE DOSE EPI TRAY, Pack Number DYNDA2965;  7) MAMMOGRAPHY TRAY, Pack Number DYNDH1094;  8) FTMC PAIN TRAY, Pack Number DYNDH1239D;  9) LUMBAR PUNCTURE - CHLORAPREP, Pack Number DYNDH1351B ;  10) PAIN MANAGEMENT PACK, Pack Number DYNDH1697;  11) PAIN MANAGEMENT PACK, Pack Number DYNDH1697A ;  12) EPIDURAL TRAY , Pack Number DYNDH1739;  13) PAIN MANAGEMENT TRAY, Pack Number DYNDH1823;  14) PAIN KIT MARSHFIELD , Pack Number DYNDH1842;  15) PAIN TRAY , Pack Number DYNDH1938;  16) PAIN SERVICE PACK-LF, Pack Number DYNJ0101290C ;  17) PAIN SERVICE PACK-LF, Pack Number DYNJ0101290D ;  18) PAIN SERVICE PACK-LF, Pack Number DYNJ0101290F ;  19) MANAGEMENT PAIN PACK-LF , Pack Number DYNJ0377378G ;  20) MANAGEMENT PAIN PACK-LF , Pac

## 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-2634-2024
- **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-2634-2024

## Citation

> AI Analytics. FDA recall Z-2634-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2634-2024. Source: US FDA. Licensed CC0.

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