medical Class II Updated 2024-10-02

Stryker Spine recalls AVS Anchor-C Cervical Cage System Instructions For Use (IFU)

Recalled Product

AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at one level from the C2-C3 disc to the C7-T1 disc.

Hazard / Issue

Labeling Correction: Instructions For Use (IFU)-Updated electronic Rev 5, specific language for indications for use for the United States and Canada was inadvertently removed.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: electronic eIFU (revision 5) Rev 5 available January 2023 to present.
View official government recall

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