Fluticasone Propionate Nasal Spray USP, 50 mcg per spray, 120 metered sprays, 16 g net fill, Rx only, Manufactured by: Apotek…
Reason CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex
22 FDA recalls mention Fluticasone. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Fluticasone.
Reason CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex
Reason CGMP Deviations: potential presence of Burkholderia cepacia complex
Reason CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Reason Defective container: defect prevents product from dispensing as intended.
Reason CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Reason CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Reason Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Reason Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Reason Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Reason Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Reason Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Reason Defective Container: Potential for broken glass in the neck area of the glass bottles.
Reason Presence of foreign substance: Potential for glass in the neck area of the glass bottles.
Reason Presence of foreign substance: glass particles
Reason CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure…
Reason Failed Stability Specifications: Out of specification for preservative, benazalkonium chloride.
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 Product Lacks Stability: These lots are being recalled due to the failure to meet the particle size distribution specification.
Reason Product Lacks Stability: These lots are being recalled due to the failure to meet the particle size distribution specification.
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.