# FDA recall Z-2408-2024

> **Canadian Hospital Specialties Ltd.** · Class II · device recall initiated 2024-06-11.

## Product

Product Name: HIGH FLOW INSUFFLATION TUBING (with Filter)  Model/Catalog Number: 20400161S  Product Description: Laparoscopic Insufflator

## Reason for recall

A customer found product with incomplete seals of P/N 20400161S, lot #185198 which can lead to non-sterile product and patient safety concerns. CHS has validated this complaint.

## Distribution

US Nationwide distribution in the state of MA.

## Key facts

- **Recall number:** Z-2408-2024
- **Recalling firm:** Canadian Hospital Specialties Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-11
- **Report date:** 2024-07-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oakville, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2408-2024

## Citation

> AI Analytics. FDA recall Z-2408-2024. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-2408-2024. Source: US FDA. Licensed CC0.

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