---
title: "Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, ... — FDA record Z-0765-2023 | Is It on Recall"
description: "Scissors contained debris."
url: https://isitonrecall.com/recall/fda-device-z-0765-2023-medical-action-industries-inc-disposable-instrument-pack-littauer-scissor-ref-56247-packaged-1-packa/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packag... — FDA record Z-0765-2023

Reported terminated

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 12, 2022. 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**: Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box, 12 boxes/case, sterile.
- **Reason**: Scissors contained debris.
- **Classification**: Class II
- **Recalling firm**: Medical Action Industries, Inc. 306
- **Quantity**: 145 cases (240 scissors/case)
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0765-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0765-2023%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 | Lot #297668, UDI 10809160003473. |

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

## Distribution

Distribution was made to FL, IL, IN, MA, MD, MO, OH, and VA. There was no foreign/government/military distribution.

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

- [Florida](https://isitonrecall.com/state/florida/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: Dec 28, 2022
- **Recall initiation date**: Oct 12, 2022
- **Center classification date**: Dec 22, 2022
- **Termination date**: Feb 19, 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-0765-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medical Action Industries, Inc. 306 records](https://isitonrecall.com/brand/medical-action-industries-inc-306/)