Assurance Infusion recalls 20mL hydromorphone syringes with lot 12162019@7 due to lack of sterility assurance. Discard or contact for details.
Lack of sterility assurance.
Assurance Infusion is recalling hydromorphone 15mg/ml injections in 20mL syringes because they may not be sterile. This could lead to infections if used improperly.
The syringes lack sterility assurance, meaning they could be contaminated with bacteria. If used, this might cause infections in patients receiving the medication.
Patients using hydromorphone injections from Assurance Infusion. Those with the specific lot number 12162019@7 are most at risk.
Check for the lot number 12162019@7 on the syringe packaging. The product was sold with expiration date 12/25/2019.
Look for the lot number 12162019@7 on the syringe packaging.
The recall states the syringes lack sterility assurance, so they should not be used. Contact Assurance Infusion for details.
The recall does not specify a remedy, so contact Assurance Infusion at (713) 533-8800 for guidance.
Check for the lot number 12162019@7 on the syringe packaging. The product was sold with expiration date 12/25/2019.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0740-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0740-2020 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.
