Class II · Moderate risk
Taztia XT
Failed Dissolution Specification: Out of a specification result occurred during the 3-month stability testing. Dissolution result at the 4-hour time point was 41% (specification: 20-40%).
Is Diltiazem recalled?
Yes — there is an active recall. 9 ongoing FDA recalls mention Diltiazem (52 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Diltiazem. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Diltiazem recalls on record
none so far in 2026; 52 on record, newest first
Class I · High risk
Taztia XT (Diltiazem HCl)
Labeling: Label Mix Up; packages labeled as Thiamine actually contain Diltiazem Capsules
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