Tailstorm Health recalls LIDOcaine HCL Sterile Injection due to potential sterility issues from FDA inspection concerns. Affected lots expire 3/23/2026 and 3/25/2026.
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 not properly sterile.
The FDA inspection found issues with the sterile manufacturing process. This could mean the product is not sterile, potentially causing infections if used improperly.
Healthcare providers and patients using this injection for nerve blocks or epidural procedures. Those with the specific lot numbers and expiration dates listed are most at risk.
Check for the product name 'LIDOcaine HCL Sterile Injection, USP, 100mg/10mL, 1% (10mg/mL) with Epinephrine 1:100,000'. Look for lot numbers 2503004 (expires 3/23/2026) or 2503005 (expires 3/25/2026).
Identify the lot number and expiration date on the vial to determine if it's affected.
The FDA inspection found concerns with the sterile manufacturing process, which could lead to potential infections.
Check the lot number and expiration date. If it's lot 2503004 (expires 3/23/2026) or 2503005 (expires 3/25/2026), contact Tailstorm Health for guidance.
The recall is due to potential sterility issues, which could cause infections, but the remedy does not specify immediate stop-use or serious injury risks.
We’ve drafted a message you can send Tailstorm Health to request your refund or repair — edit it as you like.
Subject: Recall D-0502-2025 — Tailstorm Health Tailstorm Health Hello, I own a Tailstorm Health that is covered by recall D-0502-2025 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.
