Z-2784-2024 Class II Ongoing
FDA device recall Z-2784-2024 was initiated by Beaver Visitec International, Inc. on July 26, 2024 and is designated Class II. Reason for recall: Data in RES. The recall status is ongoing. Affected quantity: 4 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 4, 2024
- Initiation Date
- July 26, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4 units
Product Description
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584550;
Reason for Recall
Data in RES.
Distribution Pattern
US Nationwide distribution.
Code Information
Part Number: 584550; UDI-DI: 30886158140758; Lot/Batch Number: 6048601