Teligent Pharma is recalling Lidocaine Cream 4% tubes due to quality control deviations. All products within expiry are affected as the company discontinues its stability study program.
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% tubes that were distributed by Rugby Laboratories. The recall is due to the company discontinuing its stability study program, which means all products within their expiry dates are affected.
The recall is due to Teligent Pharma discontinuing its stability study program, which means the product's quality control has not been verified. This could affect the product's safety and effectiveness over time.
People who own or use Lidocaine Cream 4% tubes distributed by Rugby Laboratories are affected. Those most at risk are individuals using the product for medical purposes.
Check for the product name 'Lidocaine Cream 4%', net weight 30 grams, and the distributor Rugby Laboratories. Look for batch numbers 15722, 16274, 16947, or 17140 with specific expiry dates.
Identify the product by checking the label for 'Lidocaine Cream 4%', net weight 30 grams, and distributor Rugby Laboratories.
Teligent Pharma is recalling the product because they discontinued their stability study program, which affects the product's quality control.
The recall record does not specify any remedy steps.
Batch numbers 15722, 16274, 16947, and 17140 are affected with specific expiry dates.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0704-2022 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0704-2022 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.
