Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Medicina UK with 8 device recalls. The most recent is a device recall dated Jul 4, 2022: Medicina Oral Tip Syringe 0.5ml Code: OT005.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 4, 2022 | Medicina Oral Tip Syringe 0.5ml Code: OT005Class II · Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet r | Device recalls |
| Jul 4, 2022 | Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LDClass II · Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet r | Device recalls |
| Jul 4, 2022 | Medicina Oral Tip Syringe 2.5ml Code: OT25Class II · Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet r | Device recalls |
| Jul 4, 2022 | Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05Class II · Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet r | Device recalls |
| Jul 4, 2022 | Medicina Reusable Oral syringe 5ml Code: OTH05Class II · Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet r | Device recalls |
| Jul 4, 2022 | Medicina Oral Tip Syringe 1ml Code: OT01Class II · Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet r | Device recalls |
| Jul 4, 2022 | Medicina Reusable Oral syringe 2.5ml Code: OTH25Class II · Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet r | Device recalls |
| Jul 4, 2022 | Medicina Reusable Oral syringe 1ml Code: OTH01Class II · Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet r | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
