# FDA recall Z-2911-2020

> **C.A. Greiner & Sohne Gesellschaftmbh** · Class II · device recall initiated 2020-07-27.

## Product

Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen withdrawal from specimen collection bags or bottles through needleless cannula ports.

## Reason for recall

Sample leaking from the sleeve covering the needle inside the cannula

## Distribution

US Nationwide distribution including in the states of UT, TN.

## Key facts

- **Recall number:** Z-2911-2020
- **Recalling firm:** C.A. Greiner & Sohne Gesellschaftmbh
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-07-27
- **Report date:** 2020-09-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kremsmunster, N/A, Austria

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2911-2020

## Citation

> AI Analytics. FDA recall Z-2911-2020. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-2911-2020. Source: US FDA. Licensed CC0.

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