CLASS I Drug recall · Reported 30 Jul 2014 · FDA Enforcement Report
Taztia XT (Diltiazem HCl) Capsules, 120 mg, Rx, Packaged recalled
Shamrock Medical Solutions Group is recalling Taztia XT (Diltiazem HCl) Capsules, 120 mg, Rx, Packaged and labeled as Thiamine, distributed in Colorado, Massachusetts, Ohio, Texas, Wyoming. The recall was initiated on 27 Sep 2011 and the FDA has classified it as Class I.
Check your package
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-1446-2014
- FDA event ID
- 64611
- Recalling firm
- Shamrock Medical Solutions Group, Lewis Center, OH
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 27 Sep 2011
- FDA classified
- 23 Jul 2014
- Reported
- 30 Jul 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Packaging Defects
- Drug class
- Blood Pressure Medication
Timeline
| 27 Sep 2011 | Recall initiated by company | |
| 23 Jul 2014 | Classified by FDA | +1030 days |
| 30 Jul 2014 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Label Mix Up; packages labeled as Thiamine actually contain Diltiazem Capsules
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Taztia XT (Diltiazem HCl) Capsules, 120 mg, Rx, Packaged and labeled as Thiamine. Re-Packaged By: Shamrock Medical Solutions, Lewis Center, Ohio, Mfg: Watson Laboratories, Corona, CA NDC 62037-0696-90
Where it was distributed
Product was shipped to the following states: CO, MA, OH, TX & WY.
Questions about this recall
Is Taztia XT (Diltiazem HCl) Capsules, 120 mg, Rx, Packaged and labeled as Thiamine recalled?
Yes. Shamrock Medical Solutions Group recalled Taztia XT (Diltiazem HCl) Capsules, 120 mg, Rx, Packaged and labeled as Thiamine on 27 Sep 2011. The recall is Class I and its status is Terminated. Recall number D-1446-2014.
Why was it recalled?
Labeling: Label Mix Up; packages labeled as Thiamine actually contain Diltiazem Capsules
Which lots are affected?
Use By: 5/31/2013, Lot: 0021OC, NDC 62037-0696-90
Where was it sold?
Product was shipped to the following states: CO, MA, OH, TX & WY.
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 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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