Atlas FDA

Stryker brand Synergy extended stay stretcher; model 1050

FDA device recall Z-0304-04 · posted 2004-07-20 · Terminated

Recall details

Recalling firm
Stryker Medical
Reason for recall
Users may be pinched in the siderail assembly when raising or lowering the siderail.
Action taken
Customers were sent a recall letter dated December 30, 2003. The firm will visit each facility and modify the siderail assembly.
Root cause
Other
Status
Terminated
Product code
INK
Quantity affected
107
Distribution
United States and Colombia.
Date initiated
2003-12-30
Date posted
2004-07-20
Date terminated
2004-04-15
Location
Kalamazoo, MI

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