Medicina recalls ENFit 5ml Reusable Enteral Syringes with unapproved polyethylene plunger material. Affected units have specific batch codes. Stop using immediately to avoid potential injury.
Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification
Medicina is recalling ENFit 5ml Reusable Enteral Syringes with a plunger made from unapproved polyethylene instead of polypropylene. This could cause injury if the syringe is used improperly.
The plunger uses polyethylene instead of polypropylene, which doesn't meet material specifications. This could lead to improper function or injury if the syringe is used incorrectly.
People who own or use Medicina ENFit 5ml Reusable Enteral Syringes with the specified batch codes are affected. Healthcare professionals and patients using these syringes are most at risk.
Check the syringe for batch codes: HM17099, HM18010, HM18052, HM18103, HM18113, HM18143, HM19009, HM19018, HM19061, HM19084, HM19132, HM19146, HM20006, HM20032, HM20055, HM20095, HM21037, HM21069, HM22019.
Look for batch codes on the syringe: HM17099, HM18010, HM18052, HM18103, HM18113, HM18143, HM19009, HM19018, HM19061, HM19084, HM19132, HM19146, HM20006, HM20032, HM20055, HM20095, HM21037, HM21069, HM22019.
The plunger component uses unapproved polyethylene instead of polypropylene, which doesn't meet raw material specifications.
Check the batch code on the syringe; affected units have specific batch codes: HM17099, HM18010, HM18052, HM18103, HM18113, HM18143, HM19009, HM19018, HM19061, HM19084, HM19132, HM19146, HM20006, HM20032, HM20055, HM20095, HM21037, HM21069, HM22019.
The recall record does not specify a remedy, so contact Medicina Uk Ltd for further instructions.
We’ve drafted a message you can send Medicina to request your refund or repair — edit it as you like.
Subject: Recall Z-0108-2023 — Medicina Medicina Hello, I own a Medicina that is covered by recall Z-0108-2023 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.
