---
title: "LAPAROSCOPY PACK, Model No. CALS41F, CALS41F-01, CALS41G — FDA record Z-1331-2025 | Is It on Recall"
description: "ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment."
url: https://isitonrecall.com/recall/fda-device-z-1331-2025-laparoscopy-pack-model-no-cals41f-cals41f-01-cals41g/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# LAPAROSCOPY PACK, Model No. CALS41F, CALS41F-01, CALS41G — FDA record Z-1331-2025

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 Feb 6, 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**: LAPAROSCOPY PACK, Model No. CALS41F, CALS41F-01, CALS41G
- **Reason**: ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- **Classification**: Class II
- **Recalling firm**: American Contract Systems Inc
- **Quantity**: 303 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1331-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1331-2025%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. Model No. CALS41F UDI-DI 00191072215727 Tray Lots 962241 70-050280 70-050870 70-051556 2. Model No. CALS41F-01 UDI-DI 00191072215727 Tray Lot 70-052412 3. Model No. CALS41G UDI-DI 00191072233332 Tray Lot 70-053051 |

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

## Distribution

US Nationwide distribution in the state of OH.

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

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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Mar 26, 2025
- **Recall initiation date**: Feb 6, 2025
- **Center classification date**: Mar 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-1331-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [American Contract Systems, Inc. records](https://isitonrecall.com/brand/american-contract-systems-inc/)