# FDA recall Z-0791-2018

> **Avid Medical, Inc.** · Class II · device recall initiated 2017-06-22.

## Product

AVID TruCustom KNEE ARTHROSCOPY PACK convenience kits, Item Code: MADN011-02

## Reason for recall

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

## Distribution

Distributed in 10 states: IL, KY, LA, MA, MO, NY, OH, TX, VA, WI.

## Key facts

- **Recall number:** Z-0791-2018
- **Recalling firm:** Avid Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-22
- **Report date:** 2018-03-07
- **Termination date:** 2018-10-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Toano, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0791-2018

## Citation

> AI Analytics. FDA recall Z-0791-2018. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-0791-2018. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*