Medicina UK recalls ENFit 1ml reusable low-dose enteral syringes with unapproved polyethylene plunger material. Affected units have specific batch numbers and codes. Consumers should contact for remedy.
Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification
Medicina is recalling reusable 1ml enteral syringes that use an unapproved polyethylene plunger material instead of polypropylene. This could lead to improper function or safety issues if the syringe is used for medical purposes.
The plunger component uses polyethylene instead of polypropylene, which does not meet the required material specifications. This could cause the syringe to malfunction or fail during use, potentially leading to incorrect dosing or injury.
People who own or use Medicina ENFit 1:1ml reusable low-dose enteral syringes with the specified batch numbers and codes are affected. Healthcare workers and patients using these syringes for medical treatments are at the highest risk.
Check for the code LHE01LD on the syringe and batch numbers listed: HM17121, HM18051, HM18080, HM18120, HM18141, HM19007, HM19016, HM19059, HM19083, HM19130, HM19144, HM20005, HM20054, HM21044, HM22018.
Identify the code LHE01LD and batch numbers listed in the recall notice to confirm if your syringe is affected.
The plunger component uses an unapproved material (polyethylene instead of polypropylene) that does not meet raw material specifications.
The recall notice does not specify a remedy, so contact Medicina UK for further instructions.
Batch numbers HM17121, HM18051, HM18080, HM18120, HM18141, HM19007, HM19016, HM19059, HM19083, HM19130, HM19144, HM20005, HM20054, HM21044, HM22018.
We’ve drafted a message you can send Medicina to request your refund or repair — edit it as you like.
Subject: Recall Z-0107-2023 — Medicina Medicina Hello, I own a Medicina that is covered by recall Z-0107-2023 from Medicina. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
