# FDA recall Z-1522-2026

> **Waldemar Link GmbH & Co. KG (Mfg Site)** · Class II · device recall initiated 2026-01-12.

## Product

Endo-Model Replacement Plateau;  Item Number: 15-0027/12;

## Reason for recall

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

## Distribution

Worldwide - US Nationwide distribution in the state of NJ and the countries of Belarus, Canada, Switzerland  , Colombia, Germany, Spain, United Kingdom, Hungary, India, Italy, Netherlands, Romania, Saudi Arabia.

## Key facts

- **Recall number:** Z-1522-2026
- **Recalling firm:** Waldemar Link GmbH & Co. KG (Mfg Site)
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-12
- **Report date:** 2026-03-18

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1522-2026

## Citation

> AI Analytics. FDA recall Z-1522-2026. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1522-2026. Source: US FDA. Licensed CC0.

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