Official recall notice
FDA DeviceClass IINotable
FDA Recall: Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.
- Recall date
- 2026-04-22
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Increased rate of out-of-specification endotoxin results.
Recommended action
What to do
148 units
Product description
Increased rate of out-of-specification endotoxin results.