Wal-Fex Fexofenadine Hydrochloride tablets
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Yes — there is an active recall. 4 ongoing FDA recalls mention Histamine (109 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Histamine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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