# FDA recall Z-1791-2024

> **TriMed Inc.** · Class II · device recall initiated 2024-03-19.

## Product

TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only  TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx Only

## Reason for recall

Nail system contains an out of specification driver-socket which  could result in inability to pick up nails or apply sufficient torque.

## Distribution

US Nationwide distribution in the states of AK, AR, AZ, CA, FL, HI, IL, LA, MA, MI, NC, NJ, NV, 	OH, OK, PA, TN, TX, UT, VA, WA, WI.

## Key facts

- **Recall number:** Z-1791-2024
- **Recalling firm:** TriMed Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-19
- **Report date:** 2024-05-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Santa Clarita, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1791-2024

## Citation

> AI Analytics. FDA recall Z-1791-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1791-2024. Source: US FDA. Licensed CC0.

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