Atlas FDA

P.F.C. Knee System 7 Fluted Femoral Stem 18mmX130mm REF: 96-1731

FDA device recall Z-1370-04 · posted 2004-08-24 · Terminated

Recall details

Recalling firm
Depuy Orthopaedics, Inc.
Reason for recall
The collar was incorrectly etched for the R (right) and L (Left) orientation
Action taken
Depuy notified distributors at the various territories via verbal contact on 12/23/2003
Root cause
Other
Status
Terminated
Product code
JWH
Quantity affected
1 unit
Distribution
NY
Date initiated
2003-12-22
Date posted
2004-08-24
Date terminated
2004-09-23
Location
Warsaw, IN

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