Teligent Pharma recalls 2% Erythromycin Topical Solution USP 60mL (Rx Only) due to failed impurities/degradation specs. This prescription medication may contain harmful levels of impurities.
Failed Impurities/Degradation Specifications
Teligent Pharma is recalling prescription Erythromycin Topical Solution USP 2% 60mL products because they failed impurities and degradation specifications. This means the medication may contain harmful levels of impurities that could cause health risks.
The medication failed impurities and degradation specifications, meaning it may contain harmful levels of impurities. This could potentially cause health risks if the medication is used as intended. The exact health risks are not specified in the recall notice.
Prescription patients who have received this specific Erythromycin Topical Solution USP 2% 60mL product (NDC 52565-027-59, Lot 14180) from Teligent Pharma in Buena, NJ. Patients using this medication for skin infections are most at risk.
Check for the product name 'Erythromycin Topical Solution USP 2% 60 mL', prescription label, and the NDC number 52565-027-59 with Lot 14180. This product was manufactured by Teligent Pharma in Buena, NJ.
Look for the NDC number 52565-027-59 and Lot 14180 on the product label.
The recall states the product failed impurities and degradation specifications, but does not specify if it is safe to use. The manufacturer has not provided a remedy.
The recall does not provide a specific remedy or action steps for affected products.
Check for the NDC number 52565-027-59 and Lot 14180 on the product label. This product was manufactured by Teligent Pharma in Buena, NJ.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0689-2021 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0689-2021 from Teligent Pharma. 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.
