[Recalled] Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05 — Plunger component has been manufactured with an unapproved material (Polyethyle… | FDA 2022-07-04

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification

This Class II recall concerns device products distributed in United Kingdom and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Medicina Uk Ltd

• Medicina Oral Tip Syringe 0.5ml Code: OT005 — Class II
• Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD — Class II
• Medicina Oral Tip Syringe 2.5ml Code: OT25 — Class II
• Medicina Reusable Oral syringe 5ml Code: OTH05 — Class II
• Medicina Oral Tip Syringe 1ml Code: OT01 — Class II
• Medicina Reusable Oral syringe 2.5ml Code: OTH25 — Class II

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.