Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
25 gauge VersaVit 2.0 Procedure Pack with Photon Wide Field Illuminator Recalled by Synergetics Inc Due to Vitrectomy cutters have been found not to be...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Synergetics Inc directly.
Affected Products
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.
Quantity: 255 units
Why Was This Recalled?
Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
Where Was This Sold?
This product was distributed to 14 states: AL, CA, IN, KY, MI, MS, NJ, NY, OH, SC, TN, TX, UT, VA
About Synergetics Inc
Synergetics Inc has 37 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report