Apollo Care recalls Fentanyl 50 mcg/mL syringes due to lack of assurance of sterility. This could lead to infections if used improperly. Affected units have specific NDC and lot numbers.
Lack of Assurance of Sterility
Apollo Care is recalling Fentanyl 50 mcg/mL syringes (NDC 71170-910-25) because they may not be sterile. Using these syringes could cause infections, especially for patients receiving medical injections.
The syringes lack assurance of sterility, meaning they might be contaminated with bacteria. If used for injections, this could lead to infections or other health complications.
Patients prescribed Fentanyl injections by a doctor who own this specific syringe model are affected. Those with medical conditions requiring precise dosing are at higher risk.
Check for the NDC number 71170-910-25 and lot number AC-016624 on the syringe. These syringes were sold with an expiration date of June 10, 2023.
Look for the NDC number 71170-910-25 and lot number AC-016624 on the syringe.
The recall states the syringes lack assurance of sterility, so they are not safe for medical use.
Check for NDC 71170-910-25 and lot number AC-016624 on the syringe.
The recall does not specify a remedy, so contact Apollo Care directly for guidance.
We’ve drafted a message you can send Apollo Care to request your refund or repair — edit it as you like.
Subject: Recall D-0634-2023 — Apollo Care Apollo Care Hello, I own a Apollo Care that is covered by recall D-0634-2023 from Apollo Care. 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.