30 FDA recalls mention Cetirizine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Cetirizine.
Reason Failed Impurities/Degradation Specifications: out of specification results for impurities/degradation testing for N-Oxide
Reason Failed Impurities/Degradation Specifications: out of specification results for impurities/degradation testing for N-Oxide
Reason Failed impurities/degradation specifications; out of specification for the known impurity 4-chlorobenzophenone.
Reason Labeling: Label Mixup: CETIRIZINE HCL, Tablet, 5 mg may have potentially been mislabeled as the following drug: LITHIUM CARBONATE ER, Tablet, 300…
Reason Impurity/Degradation; exceeded impurity specification at the 8 and 15 month time points (betacyclodextrin ester 1&2)
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