Synergetics 25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number recall — FDA Z-0119-2017
Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
Overview of recall records associated with Synergetics Inc., including dates, categories and classifications where available.
Classification mix: Class II: 4.
Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
This page summarizes recall records in which the official source identifies Synergetics 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.