# FDA recall Z-3120-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-06-27.

## Product

Medline convenience kits containing semi-rigid suction liners labeled as follows:    a) AMB VITRECTOMY, Pack Number DYNJ59921B;   b) AMB VITRECTOMY, Pack Number DYNJ59921BH;   c) AMB OCULOPLASTICS MUSC, Pack Number DYNJ59923B;   d) AMB OCULOPLASTICS MUSC, Pack Number DYNJ59923BH;   e) AMB CUSTOM EYE, Pack Number DYNJ59924B;   f) AMB CUSTOM EYE, Pack Number DYNJ59924BH;   g) CATARACT-30843, Pack Number DYNJVB91139

## Reason for recall

XXX

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Panama.

## Key facts

- **Recall number:** Z-3120-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-27
- **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-3120-2024

## Citation

> AI Analytics. FDA recall Z-3120-2024. Retrieved 2026-09-10 from https://api.ai-analytics.org/recall/Z-3120-2024. Source: US FDA. Licensed CC0.

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