53 FDA recalls mention Iron. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Iron.
Reason Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.
Reason Lack of Assurance of Sterility
Reason cGMP Deviations: Products may have microbial contamination.
Reason cGMP Deviations: Products may have microbial contamination.
Reason Failed Stability Specification: out of specification for iron content.
Reason Microbial contamination
Reason Microbial contamination
Reason Microbial contamination
Reason Microbial contamination
Reason CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Reason Labeling: Labeling Error on Declared Strength; The outer carton (secondary packaging) statement of ingredients misstates the concentration of active…
Reason Failed Stability Specifications: Product stability testing results did not meet specifications for iron content.
Reason Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.
Reason Subpotent Drug: Product has an an out of specification in iron assay analysis found during 18 month stability testing.
Reason Lack of Processing Controls
Reason Lack of Assurance of Sterility and Stability Data does not Support Expiry: recent inspection observations associated with certain quality control…
Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…
Reason Marketed without an Approved NDA/ANDA; Product contains unapproved hHCG.
Reason Crystallization; visible crystals from the active ingredient formed due to extreme cold temperatures during shipping
Reason Marketed without an Approved NDA/ANDA: This recall is being initiated because of changes to the dissolution profile in distributed lots resulting…
Reason Marketed without an Approved NDA/ANDA: This recall is being initiated because of changes to the dissolution profile in distributed lots resulting…
Reason Marketed without an Approved NDA/ANDA: This recall is being initiated because of changes to the dissolution profile in distributed lots resulting…
Reason Labeling: Label Mixup: MULTIVITAMIN/MULTIMINERAL W/IRON, CHEW Tablet, 0 mg may have potentially been mislabeled as the following drug…
Reason Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL LOW IRON Tablet may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 112 mcg, NDC…
Reason Labeling: Label Mixup; FERROUS SULFATE, Tablet, 325 mg (65 mg Elemental Iron) may be potentially mislabeled as RAMIPRIL, Capsule, 2.5 mg, NDC…
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.