ClearanceBrief
Recall Z-0071-2014 ยท KWA Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)

Zimmer, Inc.

Metasul Head. Intended for use either with or without bone cement in total hip arthroplasty.

DateOct 25, 2013 (initiated Aug 30, 2013)
StatusTerminated
ReasonThe low density polyethylene (LDPE) bag used to package implants adheres to the highly polished surface of the devices.
Root causePackage design/selection
ActionAugust 30, 2013 Urgent Recall Notices were sent to Distributors, hospital risk managers and surgeons identifying the issue and directing consignees to make all affected personnel aware of the contents of the notification. The notice identified the products involved, the issue, possible adverse events associated with the issue and recommended that implants found with LDPE bag adhesion not use the product and return it to Zimmer sales representatives. Questions or concerns should be addressed to Zimmer customer call center at 1-877-946-2761 between the hours of 8 a.m. and 5 p.m. EST.
Quantity194 (8770-040)
DistributionWorldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Dominican Republic, Ecuador, El Salvador, Germany, Guatemala, Honduras, Hong Kong, India, Israel, Jamaica, Japan, Korea, Malaysia, Mexico, New Zealand, Nicarag
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K091973METASUL TAPER LINERS, METASUL FEMORAL HEADS
Zimmer GmbH, Nov 17, 2009