Atlas FDA

Stryker Secure II hospital bed; model 3002.

FDA device recall Z-0868-03 · posted 2003-06-12 · Terminated

Recall details

Recalling firm
Stryker Medical
Reason for recall
A wire may break at the crimp and present a potential electric shock hazard.
Action taken
The firm sent service representatives to the receiving hospitals, beginning on 5/1/02, and the beds were corrected in place.
Root cause
Other
Status
Terminated
Product code
FNL
Quantity affected
6
Distribution
Pennsylvania and Kansas
Date initiated
2003-05-01
Date posted
2003-06-12
Date terminated
2003-06-11
Location
Kalamazoo, MI

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