87 FDA recalls mention Phoenix. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Phoenix.
Reason Lack of assurance of sterility for injectables and solutions intended to be sterile.
Reason Lack of assurance of sterility for injectables and solutions intended to be sterile.
Reason Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Reason Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals…
Reason Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals…
Reason Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals…
Reason Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals…
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Reason Crystallization: Formation of crystals observed in product.
Reason Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling bevacizumab and vancomycin due to concerns of sterility assurance with the…
Reason Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling bevacizumab and vancomycin due to concerns of sterility assurance with the…
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