Assurance Infusion recalls 20mL hydromorphone syringes with lot 12122019@17 due to lack of sterility. Discard unused syringes to prevent infection risks.
Lack of sterility assurance.
Assurance Infusion is recalling hydromorphone 20mg/ml injection syringes that may not be sterile. Using these syringes could lead to infections if they are not properly sterilized.
The syringes lack sterility assurance, meaning they might not be clean enough to prevent infections. This could happen if the syringes were not properly sterilized during manufacturing.
Patients using hydromorphone injections with this specific syringe model are affected. Healthcare providers and patients who have the lot number 12122019@17 are most at risk.
Check for the lot number 12122019@17 on the syringe packaging. The product was sold with an expiration date of December 21, 2019.
Immediately throw away any unused hydromorphone syringes with lot number 12122019@17.
The lot number is 12122019@17.
Look for the lot number 12122019@17 on the syringe packaging.
Discard unused syringes with lot number 12122019@17 immediately.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0742-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0742-2020 from Assurance Infusion. 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.
