ClearanceBrief
Recall Z-2240-2008 ยท DZE Implant, Endosseous, Root-Form

Nobel Biocare USA LLC

NobelReplace Tapered Groovy RP 4.3x10mm. These products are root-form endosseous implants intended to be surgically placed in the bone of the upper or lower jaw arches to support for prosthetic devices.

DateSep 19, 2008 (initiated Nov 2, 2007)
StatusTerminated
ReasonThis recall was initiated after it was discovered that the NobelReplace Tapered Groovy RP 4.3x10mm, REF 32216 Lot#403504 has an incorrect cap label. The affected lot has a cap label identifying the implant as "4.3x8". Since this cap label may be the only means used for identifying the implant prior to surgery, it is possible that a user would try to use the 10mm implant as an 8mm implant.
Root causeLabeling mix-ups
ActionThe recall was initiated on 11/02/2007 with telephone calls to the affected customers. A "Urgent Medical Device Recall" letter with attached Customer Response form was then sent via US Postal Service beginning on 11/02/2007. The letter instructed customers to please immediately remove and return REF 32216 Lot #403504, NobelReplace Tapered Groovy RP 4.3x10mm. The firm contracted UPS courier service to pick up the recalled products. Customers were also instructed if the have further distributed the affected product to please immediately notify those customer to cease using this particular lo
Quantity197
DistributionAR, AZ, CA, CO, FL, GA, IA, IL, MA, ME, MI, MO, NC, NC, NJ, NY, OK, PA, TX, UT, VA, WA
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K050258GROOVY IMPLANTS
Nobel Biocare AB, Apr 19, 2005
K050705TIUNITE IMPLANTS
Nobel Biocare AB, May 19, 2005