Tailor Made Compounding recalls 30ml Procaine HCL 2% vials with lack of sterility assurance. Affected batches expire by April 2022 or May 2022. Check your vial batch number for recall.
Lack of Assurance of Sterility
Tailor Made Compounding is recalling certain procaine HCL 2% vials due to a lack of sterility assurance. This could lead to infections if the medication is used. Affected vials have specific batch numbers and expiration dates.
The vials lack assurance of sterility, meaning they could be contaminated with bacteria. If used for injections, this contamination could cause infections or other health issues. The risk is not specified in the recall notice.
People who have procaine HCL 2% vials with batch numbers 10112102A2 (expiring April 2022), 11302101A1 (expiring May 2022), or 01242201A1 (expiring May 2022) are affected. Medical professionals using these vials for injections are most at risk.
Check the batch number on the vial: 10112102A2 (expires 4/9/2022), 11302101A1 (expires 5/29/2022), or 01242201A1 (expires 5/31/2022). The vials are labeled as Procaine HCL 2% (20mg/mL), 30 ml, and require refrigeration.
Look for batch numbers 10112102A2, 11302101A1, or 01242201A1 on the vial label.
The vials lack assurance of sterility, which could lead to contamination and infection if used for injections.
Check the batch number: 10112102A2 (expires 4/9/2022), 11302101A1 (expires 5/29/2022), or 01242201A1 (expires 5/31/2022).
The recall notice does not specify a remedy, so contact the manufacturer for guidance.
We’ve drafted a message you can send Tailor Made Compounding to request your refund or repair — edit it as you like.
Subject: Recall D-1222-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1222-2022 from Tailor Made Compounding. 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.
