medical Class II Updated 2021-06-09

K2M, Inc recalls Cascadia AN Interbody Convex 10x22x14mm Catalog Number: 610

Recalled Product

Cascadia AN Interbody Convex 10x22x14mm Catalog Number: 6101-2102214NC-G2 Lumbar implants are intervertebral body fusion devices indicated for use with autograft and/or allogenic bone graft comprised of cancellous and/or corticocancellous bone graft when used as anadjunct to fusion in patients with degenerative disc disease.

Hazard / Issue

Mislabeled product labeling references incorrect length or height, or length and height for specific Lots, Sizes 10x22x14mm, 10x28x14mm, 10x22x15mm

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot Number: NCMR-4437922 Expiration Date 12-10-2025
View official government recall

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