PlainRecalls
FDA Devices Moderate Class II Ongoing

Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD

Reported: October 26, 2022 Initiated: July 4, 2022 #Z-0107-2023

Product Description

Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD

Reason for Recall

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

Details

Recalling Firm
Medicina Uk Ltd
Units Affected
9 boxes (900 syringes)
Distribution
Nationwide
Location
Bolton, N/A

Frequently Asked Questions

What product was recalled?
Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD. Recalled by Medicina Uk Ltd. Units affected: 9 boxes (900 syringes).
Why was this product recalled?
Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification
Which agency issued this recall?
This recall was issued by the FDA Devices on October 26, 2022. Severity: Moderate. Recall number: Z-0107-2023.