FDA recall Z-0941-2018

Howmedica Osteonics Corp. · Class II · device

Product

Accolade and Restoration hip product; Catalog Number: 6021-0030, 6276-1-127, 6276-5-216, 6020-2530, 6020-4535, 6021-0740, 6021-0230, and 6021-4535

Reason for recall

Inner and outer sterile barriers not fully sealed.

Distribution

Distributed in ten (10) states: AR, DE, FL, IL, IN, MI, NJ, OH, TN, and TX; and Canada, Sweden, United Kingdom, France, Spain, Italy, Japan, Romania, Colombia, Netherlands, and Australia.

Key facts

Status
Terminated
Initiation date
2017-07-21
Report date
2018-03-21
Termination date
2020-03-12
Voluntary/Mandated
Voluntary: Firm initiated
Location
Mahwah, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0941-2018