Aurolife Pharma recalls 1 mg Glycopyrrolate tablets due to glass fragments in sealed bottles. This risk requires immediate action to avoid potential injury.
Presence of Foreign Substance: Complaint for pieces of glass discovered in a sealed bottle which came from equipment within the packaging room.
Aurolife Pharma is recalling 100-count bottles of 1 mg Glycopyrrolate tablets after complaints about glass pieces found in sealed bottles. This could cause injury if the tablets are swallowed or ingested.
Glass fragments in sealed bottles could be ingested if the tablets are swallowed. This poses a risk of injury to the mouth, throat, or digestive tract.
Prescription users of Glycopyrrolate tablets who received this specific batch from Aurolife Pharma. Those with medical conditions requiring this medication are most at risk.
Check for the 100-count bottle labeled 'Glycopyrrolate Tablets, USP, 1 mg' with NDC 13107-014-01. The lot number 01421008A1 was produced for this recall.
Inspect the bottle for any glass pieces before use. If found, stop using the tablets immediately.
No, the presence of glass fragments in sealed bottles makes these tablets unsafe for use. They should not be ingested.
Look for the 100-count bottle with NDC 13107-014-01 and lot number 01421008A1.
Check for glass fragments. If found, stop using the tablets immediately and contact your doctor.
We’ve drafted a message you can send Aurolife to request your refund or repair — edit it as you like.
Subject: Recall D-0736-2022 — Aurolife Aurolife Hello, I own a Aurolife that is covered by recall D-0736-2022 from Aurolife. 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.
