FDA Enforcement
Class II
Ongoing
smiths medical portex, Y' PIECE 15MM, REF 100/276/000
Recall: Z-0145-2025
·
Reported October 30, 2024
Enforcement
- Recall Number
- Z-0145-2025
- Event ID
- 95181
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Smiths Medical ASD Inc.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- October 30, 2024
- Initiation Date
- July 18, 2024
- Classification Date
- October 23, 2024
- Address
- 6000 Nathan Ln N, N/A, Minneapolis, MN, 55442-1690, United States
Description
smiths medical portex, Y' PIECE 15MM, REF 100/276/000
Reason
Uncertainty in the seal integrity of the sterile packaging.
Code Info
UDI/DI 35019315011003, Lot Numbers: 4131841, UDI/DI 35019315022405, Lot Numbers: 4122012, 4133227
Distribution
Worldwide distribution.
Quantity
9,133 units