Nephron recalls 5x5mL glycopyrrolate injections due to lack of sterility assurance. This could cause infections if used improperly. Check NDC 69374-903-05 and lot GL2002B.
Lack of Assurance of Sterility
Nephron is recalling glycopyrrolate injections that may not be sterile, which could lead to infections if used. This is a serious risk for patients receiving the medication.
The injections may not be sterile, meaning bacteria could enter the body during use. This poses a risk of infection, especially in medical settings where the product is administered.
Patients prescribed glycopyrrolate injections by healthcare providers. Those using the product without medical supervision are at highest risk.
Look for the product name 'Glycopyrrolate Injection, USP, 1 mg/5 mL (0.2 mg/mL), Preservative Free, 5 mL Pre-Filled Syringe' in 5 x 5 mL pre-filled syringes. Check the NDC code 69374-903-05 and lot number GL2002B (expiring 8/13/2022).
Immediately discard the recalled glycopyrrolate injections if you have them.
No, the product may not be sterile and could cause infections. Do not use.
Check for NDC code 69374-903-05 and lot number GL2002B (expiring 8/13/2022).
Discard the product immediately and contact your healthcare provider for alternatives.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0955-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0955-2022 from Nephron. 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.
