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Terminated

Stryker brand Synergy extended stay stretcher; model 1050

FDA Recall Z-0304-04 · Posted 2004-07-20

Recalling FirmStryker Medical
Recall StatusTerminated
Product CodeINK
Date Initiated2003-12-30
Date Terminated2004-04-15
Product Quantity107

Reason for Recall

Users may be pinched in the siderail assembly when raising or lowering the siderail.

Firm Action

Customers were sent a recall letter dated December 30, 2003. The firm will visit each facility and modify the siderail assembly.

Root Cause

Other

Distribution Pattern

United States and Colombia.

Official Source

View FDA Recall →

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

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