Cipla USA recalls Lanreotide Injection 120 mg/0.5 mL syringes due to potential contamination from inadequate visual inspection at manufacturing. This could lead to infections if used.
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
Cipla USA has recalled Lanreotide Injection 120 mg/0.5 mL syringes because they may not be sterile due to a manufacturing defect. This poses a risk of infection if the medication is used.
The product may not be sterile because the manufacturer's visual inspection process had deficiencies. This could lead to infections if the medication is used, but the risk is not immediate or severe.
Patients prescribed Lanreotide injections by a doctor are affected. Those using the recalled product for weight management or other medical conditions are most at risk.
Check for the product name 'Lanreotide Injection', 120 mg/0.5 mL, single-dose syringe, and the NDC code 69097-906-67. The lot numbers listed above indicate specific batches produced between May 2026 and July 2027.
Look for the NDC code 69097-906-67 and lot numbers from May 2026 to July 2027 on the product label.
The product may not be sterile due to manufacturing defects, so it is not safe to use. Patients should stop using it and contact their doctor.
Check for the NDC code 69097-906-67 and lot numbers listed in the recall notice, which range from May 2026 to July 2027.
Contact your doctor to discuss alternatives. The recall does not include a return or replacement process.
We’ve drafted a message you can send Cipla to request your refund or repair — edit it as you like.
Subject: Recall D-0423-2026 — Cipla Cipla Hello, I own a Cipla that is covered by recall D-0423-2026 from Cipla. 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.
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