ClearanceBrief
Recall Z-1364-2015 ยท JDR Staple, Fixation, Bone

Biomet, Inc.

Ziploop Button Product Usage: The Ziploop Button is a non-resorbable system intended to aid in ACL reconstructive procedure due to injury or degenerative disease

DateApr 2, 2015 (initiated Feb 26, 2015)
StatusTerminated
ReasonThe firm is recalling ToggleLocs and Ziploops manufactured in May and July of 2014 as they were not processed following a standard work process, which resulted in complaints of sterile packaging not being sealed.
Root causeEmployee error
ActionBiomet sent an Urgent Medical Device Recall Notice letter dated March 4, 2015 to affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to immediate locate and discontinued use of the product and its return to Biomet. Customers may contact Field Action Specialist, Regulatory Compliance,at (574) 372-1570.
Quantity50 Units
DistributionWorldwide Distribution: US (nationwide) Distribution in the states of:TX, GA, NM, NC and OK and the countries of: Japan, and the Netherlands.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K080088BIOMET SPORTS MEDICINE ANCHOR DEVICES AND ZIPLOOP CONSTRUCTS
Biomet Manufacturing, Inc., Jun 11, 2008
K101063SLEEVE WITH ZIPLOOP FIXATION DEVICES
Biomet Sports Medicine, Jun 23, 2010