---
title: "MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F. — FDA record Z-0510-2026 | Is It on Recall"
description: "Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals."
url: https://isitonrecall.com/recall/fda-device-z-0510-2026-medline-sterile-basic-eye-pack-16-1-ref-dynj37743d-2-ref-dynj37743f/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F. — FDA record Z-0510-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 3, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.
- **Reason**: Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.
- **Classification**: Class II
- **Recalling firm**: Medline Industries, LP
- **Quantity**: 1024 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0510-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0510-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 1) REF: DYNJ37743D: UDI/DI 10193489600124 (each), 40193489600125 (case), Lot Number 25EMI333; 2) REF: DYNJ37743F: UDI/DI 10198459390685 (each), 40198459390686 (case), Lot Number 25GMD927. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: MO

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Missouri](https://isitonrecall.com/state/missouri/)

## Dates in the source

- **Report date**: Nov 26, 2025
- **Recall initiation date**: Oct 3, 2025
- **Center classification date**: Nov 14, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0510-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medline Industries, LP records](https://isitonrecall.com/brand/medline-industries-lp/)