FDAFDA · Food and drugs·Recall number Z-0107-2023
Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD
Published October 26, 2022 · Recall initiated: July 4, 2022
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Medicina Uk Ltd
- Distributor
- Nationwide
- Lot
- UDI-DI: (01)05060278508146 Batch number: HM17121, HM18051, HM18080, HM18120, HM18141, HM19007, HM19016, HM19059, HM19083, HM19130, HM19144, HM20005, HM20054, HM21044, HM22018
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United Kingdom
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