medical Class II Updated 2024-12-11

Smith & Nephew Inc. recalls BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable

Recalled Product

BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable bone anchor.


Hazard / Issue

Sterile barrier breach due to inadequate packaging design that could not hold the geometry of the device.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Part No. 72201541, 72201542, 72203280, 72203281; UDI-DI: 03596010595072, 03596010595089, 03596010656452, 03596010656469; Batch No. 2146369, 2151242, 2151690, 2154691, 2153489, 2151692.
View official government recall

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