192 results · 10ms · Sources: EU EUDAMED, US FDA

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BVI Leos Laser and Endoscopy System. Model Number: OME6000U.

FDA Recall
Open, Classified ·Beaver-Visitec International, Inc.·Product code HQF·December 5, 2025

bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a component-non-sterile sample for evaluation purposes REF# BVI 58000587

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code OJK·October 8, 2021

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584003;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001380;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001635;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000759;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001878;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000479;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001417;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000781;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000305;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001423;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000477;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000628;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001579;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58002075;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001157;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584727;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000803;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584785;

FDA Recall
Open, Classified ·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024