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Terminated

3D Ceiling Suspension

FDA Recall Z-0987-03 · Posted 2003-07-10

Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeIZF
Date Initiated2003-04-15
Date Terminated2005-04-11
Product Quantity3504 units

Reason for Recall

the back up safety catch may not function properly

Firm Action

Letters dated 4/15/03 and 4/23/03 were issued to the accounts along with instructions on how to fix the problem.

Root Cause

Other

Distribution Pattern

The product was shipped nationwide to medical facilities.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K803130MULTIX U. BUCKY TABLE X-RAY UNITSiemens Corp. · 1981-01-28K790765MULTIGRAPHSiemens Corp. · 1979-04-26

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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