bvi CustomEyes Kit-Lafayette General Medical Center recall
bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a…
Why was bvi CustomEyes Kit-Lafayette General Medical Center recalled?
Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees bevel-down blades contain bevel-up blades
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Numbers 6032947 and 6033588 UDI: " Primary: 00886158019961 " Secondary: 30886158019962 " Tertiary: 50886158019966
- Product
- bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a…
- Recalling firm
- Beaver Visitec International, Inc.
- Quantity
- 125 eaches
- Distribution
- Nationwide Foreign: Australia Austria France Germany Netherlands Spain Japan Russia South Africa UK
- Recall date
- November 24, 2021
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)