Medicina Uk Ltd: Medical Device Recall in 2022 - (Recall #: Z-0107-2023)

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 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD

Product Classification:

Class II

Date Initiated: July 4, 2022

Date Posted: October 26, 2022

Recall Number: Z-0107-2023

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: 9 boxes (900 syringes)

Code Information:

UDI-DI: (01)05060278508146 Batch number: HM17121, HM18051, HM18080, HM18120, HM18141, HM19007, HM19016, HM19059, HM19083, HM19130, HM19144, HM20005, HM20054, HM21044, HM22018

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated