Z-0268-04

Bucky Diagnost FS Part number 9890-010-83651

Name: Z-0268-04 Bucky Diagnost FS Part number 9890-010-83651
Creator: Philips Medical Systems Sales & Service Region No. America
Published: 2003-11-18
License: https://open.fda.gov/license/

Philips North America LLC / initiated 2003-11-18 / Terminated

FDA source

Philips Medical Systems Sales & Service Region No. America began a recall of Bucky Diagnost FS Part number 9890-010-83651 on 2003-11-18. The reason FDA records is "Support chain attachment on the Bucky carriage may fail and cause the counter weights or X-ray tube to fall". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0268-04
Status: Terminated
Initiated: 2003-11-18
Posted: 2003-12-24
Terminated: 2005-04-11
Recalling firm: Philips North America LLC
Product: Bucky Diagnost FS Part number 9890-010-83651
Product code: KPR System, X-Ray, Stationary
Reason for recall: Support chain attachment on the Bucky carriage may fail and cause the counter weights or X-ray tube to fall.
FDA root cause: Other
Action: The firm mailed a letter to their customers on November 18, 2003 stating upgrades will begin November 14, 2003.
Quantity in commerce: 3 units
Distribution: The firm distributed to three medical facilities in Florida, New York and California.
Product codes and lots: Site numbers: 504495, 105355, 104447. The firm uses site numbers instead of serial numbers.

Product code KPR

K945278Class IIPhilips Bucky Diagnost FamilyPhilips Medical Systems North America, Inc. / cleared 1994-12-14

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)