Atlas FDA

Bucky Diagnost FS Part number 9890-010-83651

FDA device recall Z-0268-04 · posted 2003-12-24 · Terminated

Recall details

Recalling firm
Philips Medical Systems Sales & Service Region No. America
Reason for recall
Support chain attachment on the Bucky carriage may fail and cause the counter weights or X-ray tube to fall.
Action taken
The firm mailed a letter to their customers on November 18, 2003 stating upgrades will begin November 14, 2003.
Root cause
Other
Status
Terminated
Product code
KPR
Quantity affected
3 units
Distribution
The firm distributed to three medical facilities in Florida, New York and California.
Date initiated
2003-11-18
Date posted
2003-12-24
Date terminated
2005-04-11
Location
Bothell, WA

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Related 510(k) clearances

RecordFirmDate
PHILIPS BUCKY DIAGNOST FAMILY (K945278)Philips Medical Systems North America, Inc.1994-12-14