Medicina Uk Ltd 2022-10-26 Health serious FDA
Health · FDA · Recall #FDA-Z-0107-2023
Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD Recall
Issued October 26, 2022 · Medicina Uk Ltd
In October 2022, Medicina Uk Ltd recalled the Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification
What you should do
- 1 Stop using Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Medicina Uk Ltd to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Medicina Uk Ltd
- Category
- Health
- Recall date
- October 26, 2022
- Units affected
- Not reported
- Sold at
- Nationwide
- Recall number
- FDA-Z-0107-2023
- Made in
- United Kingdom
- Issuing agency
- FDA
In context
- Medicina Uk Ltd has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.