ClearanceBrief
Recall Z-0315-2012 ยท MAI Fastener, Fixation, Biodegradable, Soft Tissue

DePuy Mitek, Inc., a Johnson & Johnson Co.

DePuy Mitek Lupine Loop Plus w/ Orthocord Catalog #210708 The LUPINE BR Anchor System is indicated for use in soft tissue to bone fixation in association with adequate postoperative immobilization.

DateNov 30, 2011 (initiated Oct 31, 2011)
StatusTerminated
ReasonIncorrect suture configuration
Root causeEmployee error
ActionThe firm, DePuy Mitek Inc., sent an "URGENT VOLUNTARY PRODUCT RECALL"letter dated October 31, 2011 to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to not use or sell any of the identified problem products included in this recall; complete the enclosed business reply form and fax to: 1-508-828-3750 or email to: mitekcomplaints@its.jnj.com (note: It is important that we receive this business reply form, even if you have no product remaining in your inventory from the affected lots); isolate all inventory and call 1-877-379-4871
Quantity299 units
DistributionWorldwide distribution: USA (nationwide) and countries of: Austria, Australia, Brazil, Canada, Estonia,Switzerland, China, Czechoslovakia, Denmark, Spain, Finland, France, Great Britain Israel, India, Japan, Korea, Mexico, Martinique, Norway, Portugal, Sweden, Singapore, Solvonia, and Slovakia.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K062170BIOKNOTLESS AND LUPINE PLUS ANCHORS
Depuy Mitek, A Johnson & Johnson Company, Aug 22, 2006
K070925MODIFICATION TO: BIOKNOTLESS BR ANCHOR / LUPINE BR ANCHOR
Depuy Mitek, A Johnson & Johnson Company, May 2, 2007