---
title: "Synergetics I-Pack Injection Kit with Drape -For use with Ophthalmic injectio... — FDA record Z-2334-2024 | Is It on Recall"
description: "Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection."
url: https://isitonrecall.com/recall/fda-device-z-2334-2024-synergetics-i-pack-injection-kit-with-drape-for-use-with-ophthalmic-injections-model-catalog-number/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Synergetics I-Pack Injection Kit with Drape -For use with Ophthalmic injections Model/Catalog Number: 18061 — FDA record Z-2334-2024

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 Jun 5, 2024. 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**: Synergetics I-Pack Injection Kit with Drape -For use with Ophthalmic injections Model/Catalog Number: 18061
- **Reason**: Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
- **Classification**: Class II
- **Recalling firm**: MICROspecialties, Inc.
- **Quantity**: 96 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2334-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2334-2024%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 | UDI: 10841305101071 LOT: P63044983R |

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

## Distribution

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**: Jul 17, 2024
- **Recall initiation date**: Jun 5, 2024
- **Center classification date**: Jul 11, 2024

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-2334-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MICROspecialties, Inc. records](https://isitonrecall.com/brand/microspecialties-inc/)