FDAClass IJuly 30, 2014

Taztia XT recall: Labeling Error

Taztia XT (Diltiazem HCl) Capsules, 120 mg, Rx, Packaged and labeled as Thiamine. Re-Packaged By: Shamrock Medical Solutions, Lewis Center, Ohio, Mfg…

Why was Taztia XT recalled?

Labeling: Label Mix Up; packages labeled as Thiamine actually contain Diltiazem Capsules

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Use By: 5/31/2013, Lot: 0021OC, NDC 62037-0696-90

Product
Taztia XT (Diltiazem HCl) Capsules, 120 mg, Rx, Packaged and labeled as Thiamine. Re-Packaged By: Shamrock Medical Solutions, Lewis Center, Ohio, Mfg…
Recalling firm
Shamrock Medical Solutions Group LLC
Quantity
89/120 mg tablets
Distribution
Product was shipped to the following states: CO, MA, OH, TX & WY.
Recall date
July 30, 2014
Classification
Class I
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls