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Recall Observatory FDA recall evidence

Device product

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.

Z-0121-2017

August 11, 2016

Class II

Product summary

Firm
Synergetics Inc
Event
Event 74918
Status
Terminated
Classification
Class II
Quantity
255 units
Official record key
device-enforcement:Z-0121-2017

Official wording

Reason: Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.

Code information: Lot number M543990 (1 each or box of 6 each), exp 10/2018 Lot number M545780 (1 each or box of 6 each), exp 10/2018 Lot number M569020 (1 each or box of 6 each), exp 01/2019 Lot number M578140 (1 each or box of 6 each), exp 02/2019

Distribution pattern: Devices were distributed to KY, VA, TN, OH, IN, CA, NJ, NY, TX, SC, AL, MS, MI, and UT. Foreign distribution to the UK, France, Mexico, and India.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.