# FDA recall Z-1280-2022

> **New Standard Device Inc** · Class II · device recall initiated 2019-08-14.

## Product

Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A

## Reason for recall

Due to manufacturing processing error, wrench causing stripping when torqueing nuts.

## Distribution

U.S.: AZ. CT, GA, OH, and VA  O.U.S.: N/A

## Key facts

- **Recall number:** Z-1280-2022
- **Recalling firm:** New Standard Device Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-08-14
- **Report date:** 2022-06-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Antonio, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1280-2022

## Citation

> AI Analytics. FDA recall Z-1280-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1280-2022. Source: US FDA. Licensed CC0.

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