FDA recall Z-0641-2018

Allen Medical Systems · Class II · device

Product

Allen Medical Bow Frame Model A-70800. Surgical platform used to position patients for lumbar spine procedures.

Reason for recall

The base of the frame has the potential to crack when the patient is initially transferred to the Bow Frame.

Distribution

Worldwide distribution. US Nationwide, Australia, Bangladesh, Brazil, Canada, China, Denmark, France, Germany, Greece, Italy, Japan, Korea, Kuwait, Lebanon, Malaysia, Netherlands, Spain, Switzerland, Taiwan, UAE, and UK.

Key facts

Status
Terminated
Initiation date
2017-10-06
Report date
2018-02-28
Termination date
2019-04-03
Voluntary/Mandated
Voluntary: Firm initiated
Location
Acton, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0641-2018