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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