FDASeptember 28, 2015device

Exactech Acapella One Interbody Fusion Device Parallel. Orthopedic Spinal Surgery Device. Product Usage: The Acapella One Cervical Spacer System is indicated for anterior cervical interbody fusion procedures in skeletally mature patients with degenerative disc disease at one disc level from C2-T1...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Incorrect external and internal packaging labels. Exactech has identified nineteen (19) Acapella One Interbody Fusion Device Lordotic (05-090-01-1610) were packaged as Acapella One Interbody Fusion Device Parallel (05-090-02-1610)

What to do

FDA enforcement status: Terminated

Brands named

exactech

UPCs

05090021610

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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