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Open, Classified

Custom Made Device - GMRS EXTENSION Piece 40MM LEFT, 35 Deg EXT Rotated Tabs (Patient Specific); Catalog Number: C-MM100434-00;

FDA Recall Z-2732-2024 · Posted 2024-08-26

Recall StatusOpen, Classified
Product CodeJDI
Date Initiated2024-08-05
Product Quantity1 unit (OUS only)

Reason for Recall

A patient specific, custom-made device was supplied for a surgical procedure that did not match the design proposal.

Firm Action

On August 5, 2024 an URGENT MEDICAL DEVICE RECALL letter was sent to their consignee. Actions Needed: Our records indicate that you have received the affected product, and that product has already been returned to Stryker. We therefore request that you read this notice carefully and complete the following actions. 1. Complete and sign the enclosed Urgent Medical Device Recall Business Reply Form. Please assist us in meeting our regulatory obligation by emailing back the attached Urgent Medical Device Recall Business Reply Form within 5 days. We regret any inconvenience this action may cause. For questions pertaining to the recall, please email [email protected]

Root Cause

Process control

Distribution Pattern

International distribution to the country of Australia.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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