Z-2919-2024 Class II Ongoing
FDA device recall Z-2919-2024 was initiated by Beaver Visitec International, Inc. on July 26, 2024 and is designated Class II. Reason for recall: Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in some of BVI C… The recall status is ongoing. Affected quantity: 227 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
- 227 units
Product Description
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001838;
Reason for Recall
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in some of BVI CustomEyes Procedure Packs.
Distribution Pattern
US Nationwide distribution.
Code Information
Part Number: 58001838; UDI-DI: 30886158033203; Lot/Batch Number: 6069366