Teligent Pharma is recalling Lidocaine Cream 4% products due to cGMP deviations. All recalled items were manufactured with incomplete stability testing. Consumers should check product labels for NDC codes and batch numbers.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Teligent Pharma is recalling Lidocaine Cream 4% products because the company discontinued its stability testing program, which could affect product safety. This recall affects specific tube sizes and batch numbers produced between 2022 and 2023.
The recall is due to cGMP (current Good Manufacturing Practice) deviations where the company stopped its stability testing program. This means the product's safety and effectiveness could be compromised over time, but there is no immediate risk of injury or harm in normal use.
People who own or use Lidocaine Cream 4% products with the specified NDC codes and batch numbers are affected. Those with the highest risk are individuals using the product for medical purposes who may have been exposed to the recalled batches.
Check for Lidocaine Cream 4% tubes labeled with NDC codes 52565-122-15 (15g), 52565-122-30 (30g), or 52565-122-07 (5x5g). Also look for batch numbers from 15067 to 17023 with expiration dates between February 2022 and June 2023.
Look for NDC codes 52565-122-15, 52565-122-30, or 52565-122-07 on the tube packaging.
Teligent Pharma is recalling Lidocaine Cream 4% products because they discontinued their stability testing program, which could affect product safety.
Check the product label for the NDC codes and batch numbers listed in the recall notice. If it matches, you should stop using it and contact Teligent Pharma for further instructions.
The recall is due to manufacturing deviations, but there is no immediate risk of injury or harm in normal use. The product is safe for use as long as it has not expired.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0693-2022 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0693-2022 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.
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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.
