ClearanceBrief
Recall Z-1685-2026 ยท LCJ Tissue Expander And Accessories

Mentor Texas, LP.

Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High & Ultra High Profile, Integral Injection Dome, 300cc, 375cc, 535cc, 475cc, 500cc, 600cc, 750cc,

DateMar 27, 2026 (initiated Feb 18, 2026)
StatusOpen, Classified
ReasonInfusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
Root causeUnder Investigation by firm
ActionOn March 2, 2026, Mentor Worldwide LLC issued a updated "Urgent Medical Device Recall (Removal). The initial notification was issued on February 18, 2026. Mentor is asking consignees to take the following actions: 1. Examine your inventory and quarantine immediately any affected products. 2. Please maintain a copy of the notice with the quarantined product. 3. Notify all personnel who need to be made aware of the recall. 4. Complete the Business Reply Form of this notice and fax 877-223-7559 or email ethicon3910@sedgwick.com to Sedgwick within 3 business days. 5. If you require any assista
DistributionWorldwide distribution - US Nationwide and the countries of Canada, Albania, Australia, Austria, Belgium, Bulgaria, Croatia, Denmark, Finland, France, Germany, Iceland, Ireland, Italy, Norway, Pakistan, Poland, Romania, Saudi Arabia, Singapore, Slovakia, Slovenia, Spain, Sweden, Switzerland, Tai
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K150777Artoura Breast Tissue Expander
Mentor Worldwide, LLC, Apr 24, 2015