[Recalled] Medicina Oral Tip Syringe 1ml Code: OT01 — Plunger component has been manufactured with an unapproved material (Polyethyle… | FDA 2022-07-04
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Medicina Oral Tip Syringe 1ml Code: OT01 |
|---|---|
| Brand / manufacturer | Medicina Uk Ltd |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0110-2023 |
| Country of notice | United Kingdom |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 04 July 2022 |
| EAN / barcode | 05060278503424 |
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
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.
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