ClearanceBrief
Recall Z-1917-2017 ยท KDG Chisel (Osteotome)

Smith & Nephew, Inc.

RENOVATION, THIN OSTEOTOME BLADE, 8 MM X 5 INCH, REF 71369408, STERILE R, QTY: (1)

DateMar 30, 2017
StatusTerminated
ReasonThe stability data does not support the product labeled with a 10-year shelf life.
Root causeError in labeling
ActionThe firm initiated their recall by email and letter on 03/30/2017. Consignees were asked to inspect inventory to locate and quarantine affected product. All consignees are asked to complete a Response Form provided with the Field Safety Notice, regardless whether they have affected product. Affected inventory is then to be returned back to Smith & Nephew.
Quantity3748 units
DistributionNationwide and Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Denmark, Estonia, Finland, France, Great Britain, India, Italy, Japan, Mexico, Netherlands, Norway, Poland, Puerto Rico, Russia, Singapore, South Africa, Spain, Sweden, Switzerland, Thailand, Trinidad & Tobago, United A
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.