Assurance Infusion recalls BUP 30MG/FENT 750MCG/HYDROM 15MG syringes due to lack of sterility. This could lead to infections if used improperly. Contact the manufacturer for details.
Lack of sterility assurance.
Assurance Infusion is recalling a specific type of syringe that may not be sterile, which could cause infections if used. This is a serious issue for patients needing injections.
The syringe may not be sterile, meaning it could introduce harmful bacteria into the body during injections. This can lead to infections, especially in vulnerable individuals.
Patients using this syringe for medical injections are affected. Those with compromised immune systems are at higher risk.
Check for the product name 'BUP 30MG/FENT 750MCG/HYDROM 15MG/ML (40) INJ in 20 mL syringe' from Assurance Infusion. The lot number 12202019 and expiration date 12/20/2019 are also associated with this recall.
Identify the product name and lot number to confirm if your syringe is recalled.
The recall states there is a lack of sterility assurance, so it is not safe to use.
The recall record does not specify a remedy or replacement process.
The recall record does not provide specific instructions for action.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0702-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0702-2020 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.
