# FDA recall Z-1258-2024

> **Waldemar Link GmbH & Co. KG (Mfg Site)** · Class II · device recall initiated 2024-01-29.

## Product

Embrace Drill Tower, Standard/Lateral (25mm)

## Reason for recall

The surgical techniques for the Embrace Shoulder Instruments -Drill Tower (Article REF 645-081/62 & /63) have mixed-up type descriptions ("standard" vs "wedged") in the overview of the instruments.

## Distribution

US Nationwide distribution in the states of AL and LA.

## Key facts

- **Recall number:** Z-1258-2024
- **Recalling firm:** Waldemar Link GmbH & Co. KG (Mfg Site)
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-29
- **Report date:** 2024-03-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Norderstedt, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1258-2024

## Citation

> AI Analytics. FDA recall Z-1258-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1258-2024. Source: US FDA. Licensed CC0.

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