FDA Enforcement
Class II
Ongoing
Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD
Recall: Z-0107-2023
·
Reported October 26, 2022
Enforcement
- Recall Number
- Z-0107-2023
- Event ID
- 90849
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Medicina Uk Ltd
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Report Date
- October 26, 2022
- Initiation Date
- July 4, 2022
- Classification Date
- October 20, 2022
- Address
- Unit 2, Rivington View Business Park, Bolton, N/A, N/A, United Kingdom
Description
Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD
Reason
Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification
Code Info
UDI-DI: (01)05060278508146 Batch number: HM17121, HM18051, HM18080, HM18120, HM18141, HM19007, HM19016, HM19059, HM19083, HM19130, HM19144, HM20005, HM20054, HM21044, HM22018
Distribution
Nationwide
Quantity
9 boxes (900 syringes)