Leiters Health recalls specific VANCOmycin HCl PF 1.25g IV bags for possible double dosing risk. Affected units have unique lot numbers and expiration dates. Stop using immediately if you own these bags.
Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.
Leiters Health is recalling certain VANCOmycin HCl PF 1.25g IV bags that may contain a double dose of medication due to a malfunction in their filling system. This could lead to an overdose if used in medical treatment.
The semi-automated IV bag filling system can malfunction and deliver double the intended dose of VANCOmycin HCl PF. This could cause serious harm or death if administered to patients.
Healthcare professionals and hospitals that use these specific IV bags for patient treatment. Patients receiving IV medication from these bags are at risk of overdose.
Check for the lot numbers: 2331184 (exp. 02/13/2024), 2331185 (exp. 02/10/2024), 2331189 (exp. 02/20/2024), 2331191 (exp. 02/24/2024), 2331258 (exp. 03/03/2024), or 2331317 (exp. 03/15/2024). The product is labeled as VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3206.
Discontinue use of the recalled IV bags if you have them. Do not administer to patients.
VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3206, for IV use only.
Lot numbers 2331184 (exp. 02/13/2024), 2331185 (exp. 02/10/2024), 2331189 (exp. 02/20/2024), 2331191 (exp. 02/24/2024), 2331258 (exp. 03/03/2024), and 2331317 (exp. 03/15/2024).
The recall record states the remedy is null, meaning no specific remedy is provided beyond stopping use immediately.
We’ve drafted a message you can send Leiters Health to request your refund or repair — edit it as you like.
Subject: Recall D-0281-2024 — Leiters Health Leiters Health Hello, I own a Leiters Health that is covered by recall D-0281-2024 from Leiters 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.
