Medicina ENFit recall
Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD
Why was Medicina ENFit recalled?
Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: (01)05060278508146 Batch number: HM17121, HM18051, HM18080, HM18120, HM18141, HM19007, HM19016, HM19059, HM19083, HM19130, HM19144, HM20005, HM20054, HM21044, HM22018
- Product
- Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD
- Recalling firm
- Medicina Uk Ltd
- Quantity
- 9 boxes (900 syringes)
- Distribution
- Nationwide
- Recall date
- October 26, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)