Isomeric Pharmacy Recalls Triamcinolone Vials Due to Labeling Errors
Isomeric Pharmacy recalls 114 vials of Triamcinolone Diacetate Injectable Suspension due to incorrect or missing lot and expiration dates on labels.
Use caution until it’s fixed
Labeling: Incorrect or Missing Lot and/or Exp Date: some vials may be mislabeled with an incorrect "Compounded" date, lot number, and "Do Not Use Beyond " date or BUD (Before Use Date) that may be longer than intended.
Contact the company
What happened, in plain English
Isomeric Pharmacy Solution, LLC is recalling a small batch of Triamcinolone Diacetate Injectable Suspension because the labeling may contain incorrect or missing information. Specifically, some vials might have wrong compounded dates, lot numbers, or 'Do Not Use Beyond' dates that are longer than intended. This recall affects 114 vials distributed nationwide. Read more at govinfonow.com/recall/43202-isomeric-pharmacy-recalls-triamcinolone-vials-due-to-labeling-errors.
Source Summary by GovInfoNow · govinfonow.com/recall/43202-isomeric-pharmacy-recalls-triamcinolone-vials-due-to-labeling-errors · Updated October 11, 2026 · FDA enforcement record: FDA #D-0728-2016
Cite this page
“Isomeric Pharmacy Recalls Triamcinolone Vials Due to Labeling Errors.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43202-isomeric-pharmacy-recalls-triamcinolone-vials-due-to-labeling-errors. Based on FDA recall #D-0728-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0728-2016%22&limit=1).
Why it’s dangerous
The primary hazard is labeling errors that could lead to the use of medication past its intended safety date. If the 'Do Not Use Beyond' date is incorrect or missing, there is a risk that the compounded drug is used when it may no longer be sterile or effective.
Who’s affected
Patients who received Triamcinolone Diacetate Injectable Suspension from Isomeric Pharmacy Solution, LLC between December 2015 and March 2016. Healthcare providers or patients holding the specific lot number listed in the record are most at risk.
How to tell if you have this one
Check for Triamcinolone Diacetate Injectable Suspension, 40 mg/mL, 10mL Multi-Dose Vial for Injection, Rx only, manufactured by Isomeric Pharmacy. Look specifically for Lot Number: 12212015@8 and a 'Compounded on' date of December 21, 2015.
- Brand
Isomeric Pharmacy- Category
Drug
What to do — step by step
Check Your Vial Label
Verify if your vial matches Lot Number 12212015@8 and was compounded on December 21, 2015.
Contact Your Provider
If you have the recalled lot, contact your healthcare provider or pharmacist immediately for guidance on disposal or replacement.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #D-0728-2016 (February 2, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0728-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.