Medicina recalls 1ml reusable oral syringes with unapproved polyethylene plunger material. Affected units may not meet safety standards; 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 oral syringes that use an unapproved polyethylene plunger instead of the required polypropylene. This could lead to safety issues if the plunger fails during use.
The plunger is made from polyethylene instead of polypropylene, which may not meet safety specifications. This could cause the plunger to fail during use, potentially leading to safety issues.
Users of Medicina reusable oral syringes with the OTH01 code and batch numbers HM18041 or HM21053 are affected. People using these syringes for medical purposes are most at risk.
Check for the OTH01 code on the syringe. Affected units have batch numbers HM18041 or HM21053. The UDI-DI code is (01)05056115402869.
Look for the OTH01 code and batch numbers HM18041 or HM21053 on the syringe.
The plunger is made from polyethylene instead of the required polypropylene material, which may not meet safety specifications.
Check for the OTH01 code and batch numbers HM18041 or HM21053 on the syringe.
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-0112-2023 — Medicina Medicina Hello, I own a Medicina that is covered by recall Z-0112-2023 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.
