Teligent Pharma recalls 1.5% diclofenac topical solution bottles due to defective container risk. Rx-only product with specific lot numbers and expiration dates.
Defective Container
Teligent Pharma is recalling diclofenac sodium topical solution bottles because the container may be defective. This could lead to improper storage or handling risks for users who need this prescription medication.
The container may be defective, which could lead to improper storage or handling. This might cause the medication to be exposed to conditions that could affect its safety or effectiveness.
Prescription users of diclofenac topical solution who purchased the recalled bottles with specific lot numbers and expiration dates. Those with the product in their possession are most at risk.
Check for plastic bottles labeled 'Diclofenac Sodium Topical Solution USP, 1.5 w/w, 5 fl oz (150 mL)' with lot numbers 15028 (expiring 1/2023) or 15379 (expiring 3/2023).
Identify the lot number and expiration date on the bottle to confirm if it's in the recall list.
The recall is for defective containers, not the medication itself. If you have the product, check the lot number to see if it's recalled.
Check the lot number and expiration date on the bottle. If it matches the recalled numbers (15028 exp 1/2023 or 15379 exp 3/2023), contact Teligent Pharma for instructions.
The recall record does not specify a replacement process. Contact Teligent Pharma directly for assistance.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0259-2022 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0259-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
