Overview of recall records associated with Neotract Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
There is the potential that during implant deployment, the device may not properly deliver a implant.
Upon implant deployment, the Capsular Tab may not be delivered as the needle is retracted. In this failure mode, the needle is deployed into the prostate and retracted, leaving no implant…
This page summarizes recall records in which the official source identifies Neotract Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
