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Allergan Inc recalls Natrelle CUI Series Tissue Expanders. Product Usage: Natrelle CUI Series Tissue Expander has been designed for tempo
Recalled July 29, 2015 · FDA recall Z-2104-2015 · Allergan
Hazard
Allergan is recalling the NATRELLE 133 and CUI Series Tissue Expanders because the products shipped were beyond the shelf life. · FDA Class II
Units
23 units total (16 units in US)
Sold at
US in the state of Canada
Description
Allergan is recalling the NATRELLE 133 and CUI Series Tissue Expanders because the products shipped were beyond the shelf life.
Product
Natrelle CUI Series Tissue Expanders. Product Usage: Natrelle CUI Series Tissue Expander has been designed for temporary implantation to develop a skin flap. The device is used for reconstructive correction of a defect or to provide cover for a prosthetic implant. The CUI Tissue Expander consists of a silicone elastomer envelope and a remote injection port.
Manufacturer(s)
Allergan Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →