Tailstorm Health recalls LIDOcaine HCL Sterile Injection due to potential sterility issues found in FDA inspections. This product may not be sterile, posing infection risks during medical procedures.
Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.
Tailstorm Health is recalling LIDOcaine HCL Sterile Injection vials because an FDA inspection found concerns about the sterile manufacturing process. This could lead to infections if the product is used in medical procedures.
The FDA inspection identified potential issues with the sterile manufacturing process. This means the product might not be sterile, which could cause infections during medical procedures if used improperly.
Healthcare professionals and patients who have been prescribed this medication for nerve blocks or epidural use. Those using the product for medical procedures are at risk of infection.
Check for the product name 'LIDOcaine HCL Sterile Injection, USP, 20 mg/mL, 2%, (200 mg/10 mL)' on the vial. The lot number is 2504003 and expiration date is 04/03/2027.
Look for the lot number 2504003 and expiration date 04/03/2027 on the vial label.
The FDA found concerns with the sterile manufacturing process, so the product may not be sterile. It is recommended to stop using it if you have the specific lot number.
Check the lot number and expiration date. If you have the lot number 2504003, contact Tailstorm Health for guidance.
The recall is due to potential sterility issues, which could lead to infections. There is no mention of serious injury risks in the official notice.
We’ve drafted a message you can send Tailstorm Health to request your refund or repair — edit it as you like.
Subject: Recall D-0503-2025 — Tailstorm Health Tailstorm Health Hello, I own a Tailstorm Health that is covered by recall D-0503-2025 from Tailstorm Health. 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.
