# FDA recall Z-2995-2024

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

## Product

Medline convenience kits labeled as:   1) PERMANENT PACING, Pack Number 00-400361J ;  2) NORTON CHILDRENS CATH LAB-LF, Pack Number 00-401185Q ;  3) PACEMAKER TRAY, Pack Number 00-401521F ;  4) FEMORAL PACK, Pack Number 00-401525G ;  5) CARDIAC CATH PACK , Pack Number 00-401561K ;  6) CORONARY ANGIO PACK-LF, Pack Number 00-401594S ;  7) LEFT HEART TRAY , Pack Number 00-401880I ;  8) EP LAB PACEMAKER PACK , Pack Number 00-401893K ;  9) EP LAB PACEMAKER PACK , Pack Number 00-401893L ;  10) ADVANTEC-MLD, Pack Number 00-500510D ;  11) ADVANTEC-MLD, Pack Number 00-500510F ;  12) KIT ANGIO CSTM-WALKER, Pack Number 129969;  13) DIAGNOSTIC KIT, Pack Number 147943;  14) MSC - CRESCENT MEDICAL, Pack Number 149155;  15) VASC KIT AUGUSTA MED CEN PG , Pack Number 650123111;  16) OPEN HEART CDS, Pack Number CDS840015AK;  17) OPEN HEART CDS, Pack Number CDS840015AL;  18) OPEN HEART CDS, Pack Number CDS840015AM;  19) OPEN HEART CDS, Pack Number CDS840015AN;  20) OPEN HEART CDS, Pack Number CDS840015AO;

## Reason for recall

XXX

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-2995-2024
- **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-2995-2024

## Citation

> AI Analytics. FDA recall Z-2995-2024. Retrieved 2026-07-04 from https://api.ai-analytics.org/recall/Z-2995-2024. Source: US FDA. Licensed CC0.

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