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Synergetics Inc: Medical Device Recalls in 2016

Updated on March 25, 2026.

According to to data from the FDA, there were 4 medical device recalls made by Synergetics Inc in 2016. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2013
2014
2016
2024
  • 25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number 70025E, packaged in HIPS rigid tray with a Tyvek lid sterile barrier system.
  • 25 gauge VersaVit 2.0 Vitrectomy Cutter, Product/Part Number 70935, packaged in a Tyvek/Mylar double pouch configuration.
  • 25 gauge VersaVit 2.0 Procedure Pack with Mid-Field Illuminator, Product/Part Number 70025S, packaged in HIPS rigid tray with a Tyvek lid sterile barrier system.
  • 25 gauge VersaVit 2.0 Procedure Pack with Photon Wide Field Illuminator, Product/Part Number 70025SP, packaged in HIPS rigid tray with a Tyvek lid sterile barrier system.
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