CLASS III Drug recall · Reported 2 Mar 2016 · FDA Enforcement Report

Triamcinolone Diacetate Injectable Suspension recalled

Isomeric Pharmacy Solution is recalling Triamcinolone Diacetate Injectable Suspension, 40 mg/mL Multi-Dose Vial for Injection, distributed nationwide in the US. The recall was initiated on 2 Feb 2016 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot Number: 12212015@8, Do Not Use Beyond: 03/22/2016, "Compounded on December 21, 2015"
Quantity recalled114 vials

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0728-2016
FDA event ID
73207
Recalling firm
Isomeric Pharmacy Solution, Salt Lake City, UT
Classification
Class III
Status
Terminated
Recall initiated
2 Feb 2016
FDA classified
25 Feb 2016
Reported
2 Mar 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Labeling Errors

Timeline

2 Feb 2016Recall initiated by company
25 Feb 2016Classified by FDA+23 days
2 Mar 2016Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

Product as listed by the FDA

Triamcinolone Diacetate Injectable Suspension, 40 mg/mL, 10mL Multi-Dose Vial for Injection, Rx only, Isomeric Pharmacy Solutions, 2401 Foothill Dr., Salt Lake City, UT 84109

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

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.

Which lots are affected?

Lot Number: 12212015@8, Do Not Use Beyond: 03/22/2016, "Compounded on December 21, 2015"

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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