Telmisartan Tablets, USP 40mg, Rx Only, 30 Tablets per bottle, Manufactured by: Micro Labs Limited Goa-403 722, INDIA…
Reason Failed Stability Specifications: Out of specification for blend uniformity.
12 FDA recalls mention Telmisartan. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Telmisartan.
Reason Failed Stability Specifications: Out of specification for blend uniformity.
Reason Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the…
Reason Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the…
Reason Superpotent; Hydrochlorothiazide
Reason Subpotent Drug
Reason Labeling: Label-mixup
Reason Failed Impurities/Degradation Specifications; 18 month long term stability study (manufacturer)
Reason Failed Impurities/Degradation Specifications; 18 month long term stability study.
Reason Failed Content Uniformity Specifications: The product is out of specification for blend uniformity.
Reason Failed Content Uniformity Specifications: The product is out of specification for blend uniformity.
Reason Failed Content Uniformity Specifications: The product is out of specification for blend uniformity.
Reason Presence of Foreign Substance: Product complaint for the presence of foreign matter identified as silicone within the tablet.
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