Medicina Uk Ltd: Medical Device Recall in 2022 - (Recall #: Z-0108-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05

Product Classification:

Class II

Date Initiated: July 4, 2022

Date Posted: October 26, 2022

Recall Number: Z-0108-2023

Event ID: 90849

Reason for Recall:

Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification

Status: Ongoing

Product Quantity: 1 box (100 syringes)

Code Information:

UDI-DI: (01)05060278508153(17)250400(10)HM20055 Batch number: HM17099, HM18010, HM18052, HM18103, HM18113, HM18143, HM19009, HM19018, HM19061, HM19084, HM19132, HM19146, HM20006, HM20032, HM20055, HM20095, HM21037, HM21069, HM22019

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated