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
E-Mail
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)