Recall Z-2186-2008

Hologic, Inc. · initiated June 27, 2008

Terminated

Product

Hologic Delphi Bone Densitometers with Apex software versions 2.0, 2.1 and 2.2 is indicated for the estimate of bone mineral density, comparison of measured variables obtained from a given scan to a database of reference values, the estimation of fracture risk, vertebral deformity assessment, body composition analysis, and discrimination of bone from prosthetics.

Codes / lots: S/N: 70411W 70456W 71132C 71132C 71205W 70007C 70024C 70102C 70129C 70138C 70351C 70379A 70394A 70395C 70414A 70415A 70418A 70419A 70421A 70434W 70512A 70525W 70545W 70561W 70603W 70609C 70677C 70678W 70717C 70721W 70724A 70734A 70744C 70761C 70791C 70817W 70824C 70845C 70855SL 70896SL 70987W 71016C 71035W 71076C 71091C 71151C 71172SL 71188C 71223C 71231W 71239C 71255W 71257C 71287C 71342C and 71386C

Reason for recall

Software densitometer readings for left hip and lumbar spine under certain conditions may be inaccurate.

FDA-determined cause: Software design

Action taken

Hologic notified customers by registered letter titled Urgent: Medical Device Recall, dated 6/27/08, providing instructions to update the software to Version 2.3 and discard version APEX 2.0, 2.1 and 2.2 manuals. If you have questions or require assistance with the software installation, contact Hologic's Help Desk at 1-800-321-4659.

Details

Recall number
Z-2186-2008
Initiated
June 27, 2008
Posted by FDA
September 17, 2008
Terminated
October 25, 2010
Product code
KGI – Densitometer, Bone
Quantity
82 units
Distribution
Nationwide Foreign: Canada Algeria, AE, Australia, Belgium,China,France, Germany, Hungary, Hong Kong, Iceland, Iran, Ireland, Israel, Italy,Japan,Korea, Kuwait, Lithuania, Mexico, Myanmar, Netherlands, Pakistan, Peru, Russia, S. Africa, Saudi Arabia, Singapore, Slovak Rep., Switzerland, Syria, Taiwan, UK
Recalling firm
Hologic, Inc., Bedford, MA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2184-2008 Hologic Discovery Bone Densitometers with Apex software versions 2.0, 2.1 and 2.2 is…Software densitometer readings for left hip and lumbar spine under certain conditions may be inaccurate. 06/27/2008Terminated
Z-2185-2008 Hologic QDR4500 Bone Densitometers with Apex software versions 2.0, 2.1 and 2.2 is…Software densitometer readings for left hip and lumbar spine under certain conditions may be inaccurate. 06/27/2008Terminated
Z-2187-2008 Hologic Explorer Bone Densitometers with Apex software versions 2.0, 2.1 and 2.2 is…Software densitometer readings for left hip and lumbar spine under certain conditions may be inaccurate. 06/27/2008Terminated
Z-2188-1991 Hologic Oasis Bone Densitometers with Apex software versions 2.0, 2.1 and 2.2 is…Software densitometer readings for left hip and lumbar spine under certain conditions may be inaccurate. 06/27/2008Terminated