# FDA recall Z-2992-2024

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

## Product

Medline convenience kits labeled as:   1) ANGIOGRAPHY DRAPE PACK, Pack Number 00-398281J ;  2) ANGIOGRAPHY DRAPE PACK, Pack Number 00-398650AG;  3) ANGIOGRAPHY DRAPE PACK, Pack Number 00-398650AI;  4) ANGIOGRAPHY DRAPE PK, Pack Number 00-398712S ;  5) CATH LAB PACK , Pack Number 00-398725AM;  6) ANGIOGRAPHY DRAPE PACK, Pack Number 00-399360K ;  7) ANGIOGRAPHY DRAPE PACK, Pack Number 00-399734N ;  8) ANGIOGRAPHY DRAPE PACK, Pack Number 00-399983Q ;  9) ANGIOGRAPHY DRAPE PACK, Pack Number 00-399983R ;  10) ANGIOGRAPHY DRAPE PACK, Pack Number 00-400065K ;  11) ANGIO PROCEDURE PACK, Pack Number 00-400069F ;  12) ANGIOGRAPHY DRAPE PACK PTCA , Pack Number 00-400123AC;  13) ANGIOGRAPHY DRAPE PACK PTCA , Pack Number 00-400123AD;  14) ANGIO PROCEDURE PACK, Pack Number 00-400290D ;  15) ANGIOGRAPHY DRAPE PACK, Pack Number 00-400305Q ;  16) MOUNT SINAI HOSPITAL-ANGIO PK , Pack Number 00-400763F ;  17) ANGIOGRAPHY DRAPE PACK-LF , Pack Number 00-400863J ;  18) ANGIOGRAPHY DRAPE , Pack Number 00-400

## 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-2992-2024
- **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-2992-2024

## Citation

> AI Analytics. FDA recall Z-2992-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2992-2024. Source: US FDA. Licensed CC0.

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