Home / Recalls / Medical Devices
Allergan Inc recalls Natrelle 133 Series Tissue Expanders Product Usage: Natrelle 133 Series Tissue Expander is intended for temporary su
Recalled July 29, 2015 · FDA recall Z-2103-2015 · Allergan
Hazard
Allergan is recalling the NATRELLE 133 and CUI Series Tissue Expanders because the product shipped was beyond the 47 month shelf life. · FDA Class II
Units
167 units total (114 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 product shipped was beyond the 47 month shelf life.
Product
Natrelle 133 Series Tissue Expanders Product Usage: Natrelle 133 Series Tissue Expander is intended for temporary subcutaneous implantation and require periodic, incremental inflation with sterile saline for injection until the desired amount of tissue is developed.
Manufacturer(s)
Allergan Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →