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Terminated

Stryker Trio Mobile Surgery Platform; Model 1033.

FDA Recall Z-1155-06 · Posted 2006-06-17

Recalling FirmStryker Medical Div. of Stryker Corporation
Recall StatusTerminated
Product CodeFSE
Date Initiated2006-05-15
Date Terminated2006-07-04
Product Quantity156

Reason for Recall

An incorrect pin may have been used during assembly and therefore the device may give way during use.

Firm Action

Consignees were called on 5/15/06 and instructed to discontinue use of these devices until the firm's technician has visited the facility and replaced the pin.

Root Cause

Other

Distribution Pattern

Worldwide (including USA, Australia, Canada, England, Germany, Italy, Romania and Singapore).

Official Source

View FDA Recall →

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

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