Tailor Made Compounding recalls 25ml and 50ml ascorbic acid vials due to lack of sterility assurance. Affected batches expire by August 2022. Consumers should check batch numbers on vials.
Lack of Assurance of Sterility
Tailor Made Compounding is recalling 25ml and 50ml ascorbic acid vials that may not be sterile. This could lead to infections if used improperly. The recall affects specific batches with expiration dates up to August 2022.
The vials lack assurance of sterility, meaning they might contain harmful bacteria. If used for injections or medical purposes, this could cause infections or serious health issues. The risk depends on how the vials are used.
People who own or use the recalled ascorbic acid vials from Tailor Made Compounding. Those with medical conditions requiring sterile injections are at higher risk.
Check for batch numbers on the vial: a) 02282223A1 (exp 8/27/2022), 10112101A2 (exp 4/9/2022), etc. or b) 01042234B (exp 7/3/2022), 01242211A2 (exp 7/23/2022), etc. The vials are labeled as refrigerated.
Look for batch numbers on the vial: a) 02282223A1, 10112101A2, 11032108A1, etc. or b) 01042234B, 01242211A2, 02282222A1, etc.
The vials lack assurance of sterility, which could lead to infections if used for medical purposes.
Check the batch numbers listed in the recall notice. If you have a batch number from the list, contact Tailor Made Compounding for further instructions.
The recall indicates a lack of sterility assurance, so they may not be safe for medical use. Do not use the vials if you have a batch number from the list.
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-1195-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1195-2022 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.
