# FDA recall Z-2733-2020

> **Arthrex, Inc.** · Class II · device recall initiated 2020-06-24.

## Product

Sterile Low Profile Screw, Titanium, 6.7 x 65mm  Part Number: AR-8967-2865S - Product Usage: is intended to be used as a stand-alone bone screw, or in a plate-screw system for internal bone fixation for bone fractures, fusions, osteotomies and non-unions.

## Reason for recall

Screws provided in packaging are 5mm shorter than intended

## Distribution

International distribution in the countries of Denmark, United Kingdom, Sweden, Japan, Netherlands

## Key facts

- **Recall number:** Z-2733-2020
- **Recalling firm:** Arthrex, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-24
- **Report date:** 2020-08-05
- **Termination date:** 2021-02-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Naples, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2733-2020

## Citation

> AI Analytics. FDA recall Z-2733-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2733-2020. Source: US FDA. Licensed CC0.

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