FDA Device recall Z-1802-2015
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584569 Ophthalmic surgical kits
- FDA Device
- Class II
- terminated
- Published 2015-06-24
On 2015-06-24 the FDA classified a Class II recall of BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584569 Ophthalmic surgical kits by Beaver Visitec International, citing devon Light Glove in procedure kits may have holes/slits compromising sterility of the product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1802-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-05-01 |
| Published | 2015-06-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Beaver Visitec International |
| Distribution | US |
Product
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584569 Ophthalmic surgical kits
Reason
Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
Identifiers
| code_info | Lot Numbers: 3035614 3046205 3052693 3055885 3063181 3068806 3073917 3082315 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1802-2015%22
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