Recall Z-1810-2008
DePuy Mitek, Inc., a Johnson & Johnson Co. · initiated April 29, 2008
Product
Lupine BR Anchor w/Orthocord TCP/PLGA Absorbable Anchor, size 2 (5 metric) Braided Composite Suture, violet 36" (91cm) Size 2 (5metric) eyelet loop. Made in Switzerland; Sterile. The Lupine BR Anchor System is indicated for use in soft tissue bone fixation.
Codes / lots: Catalog Number 210711 Lot Number 3069512
Reason for recall
Lupine BR Anchor w/Orthocord was assembled with an incorrect suture configuration. The suture loop was not assembled at the distal end of the anchor. It was only threaded through the suture hole in the anchor. Risk associated with incorrect suture configuration include premature breakage.
FDA-determined cause: Employee error
Action taken
DePuy Mitek notified customers by letter dated April 29, 2008 titled Urgent: Voluntary Medical Device Recall Letter asking consignees to isolate and do not use product and to return any of the identified product to DePuy Mitek using enclosed prepaid Federal Express shipping labels and to include a photocopy of the completed Business Reply Form. The firm is asking customers to complete the Business Reply Form with a self addressed, stamped envelope indicating level of inventory of the affected product and to return for immediate delivery of replacement product. If you have any questions contact DePuy Mitek Customer Service directly at 1-800-382-4682.
Details
- Recall number
- Z-1810-2008
- Initiated
- April 29, 2008
- Posted by FDA
- September 17, 2008
- Terminated
- October 2, 2008
- Product code
- JDR – Staple, Fixation, Bone
- Quantity
- 105 units
- Distribution
- Class II Recall - Worldwide Distribution --- USA including states of CA, NY, MA, NV, OH, TX, TN, MD, and countries of France, UK, Canada, Spain.
- Recalling firm
- DePuy Mitek, Inc., a Johnson & Johnson Co., Raynham, MA