Kelyniam Global, Inc.: Medical Device Recall in 2018 - (Recall #: Z-1871-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Kelyniam Custom Skull Implant (CSI), Model no. PEEK-IM1002

Product Classification:

Class II

Date Initiated: June 10, 2017

Date Posted: May 23, 2018

Recall Number: Z-1871-2018

Event ID: 79791

Reason for Recall:

Significant design changes made to the Custom Skull Implant (CSI) devices, such as removing pressure relief holes across the length of the device and adding suture holes along the ridge of the implant, were not validated or submitted to FDA for marketing clearance. The Temporal Suture System (TSS) is no longer being offered and the Integrated Fixation System (IFS) has been temporarily suspended

Status: Terminated

Product Quantity: 16

Code Information:

Marketing Material: All revisions up to rev. A. IFU: All revisions up to rev. C. Case Numbers: CSI082114-CT1 CSI081214-TB1 CSI020216-LK1 CSI092016-LD1R CSI100116-BM1A CSI092616-YB1 CSI092616-MM1 CSI112316-YB1 CSI050217-LS1 CSI052217-AF1 CSI062317-GM1 CSI071017-NS1B CSI071417-CM1 CSI102617-DL1 CSI101617-JF1A CSI102617-DL1

Distribution Pattern:

US nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated