Official recall notice

FDA DeviceClass IINotable

FDA Recall: Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.

Recall date
2026-04-22
FDA class
Class II

Why it was recalled

Hazard

Increased rate of out-of-specification endotoxin results.

Recommended action

What to do

452 units

Product description

Increased rate of out-of-specification endotoxin results.

Verify with the official notice →
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