1,994 FDA recalls mention Chloride. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Chloride.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Lack of Assurance of Sterility: The product has the potential for solution to leak at or near the administrative port of the primary container.
Reason Discoloration: Ethambutol HCl Tablets 400 mg is being recalled due to a Out of Specification result for description testing for a surface defect of…
Reason Non-Sterility: The firm's contract testing laboratory found sterility failures.
Reason Lack of Assurance of Sterility: Specific lot numbers of these products have been identified for potential administration port leakage. The potential…
Reason Lack of Assurance of Sterilty: Specific lot numbers of these products have been identified for potential administration port leakage. The potential…
Reason Lack of Assurance of Sterility: Specific lot numbers of these products have been identified for potential administration port leakage. The potential…
Reason Lack of Assurance of Sterility: Specific lot numbers of these products have been identified for potential administration port leakage. The potential…
Reason Failed Impurity/Degradation Specifications; out of specification value for impurity Nitrophenylpuridine Derivative (NPP-D)
Reason Non-Sterility; contract laboratory identified Staphylococcus warneri in the product
Reason Subpotent; 24 month stability test station
Reason Labeling: Label Error on Declared Strength- Unopened bottles of Ropinirole USP 3 mg tablets was found to be incorrectly labeled as Ropinirole USP 4…
Reason Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.
Reason Lack of Assurance of Sterility: A mold like substance was discovered on the surface of an unopened bag of Sodium Chloride 0.9% while prepping the bag…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Subpotent; Cetylpyridinum Chloride
Reason Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates
Reason Failed USP Dissolution Test Requirements: Out-of-specification dissolution results at the 8 hour stability testing point.
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