Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Taztia XT (Diltiazem HCl) Capsules Recalled by Shamrock Medical Solutions Group LLC Due to Labeling: Label Mix Up; packages labeled as Thiamine...

Date: September 27, 2011
Company: Shamrock Medical Solutions Group LLC
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Shamrock Medical Solutions Group LLC directly.

Affected Products

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

Quantity: 89/120 mg tablets

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed to 5 states: CO, MA, OH, TX, WY

Affected (5 states)Not affected

About Shamrock Medical Solutions Group LLC

Shamrock Medical Solutions Group LLC has 6 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report