Secret OUTLAST Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Protecting Powder, Topical spray can 3.8 oz (107 g)…
Reason CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
52 FDA recalls mention Aluminum. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Aluminum.
Reason CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Reason CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Reason Chemical contamination: presence of benzene
Reason CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Reason Chemical contamination: presence of benzene
Reason Chemical contamination: presence of benzene
Reason Chemical contamination: presence of benzene
Reason Chemical contamination: presence of benzene
Reason Chemical contamination: presence of benzene
Reason CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Reason Chemical contamination: presence of benzene
Reason CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Reason CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Reason Temperature Abuse: Prolonged exposure to temperatures outside of labeled storage conditions.
Reason Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point
Reason CGMP Deviations: Cylinders filled using out of date gauges.
Reason cGMP Deviations; product does not comply with cGMP requirements
Reason cGMP Deviations; product does not comply with cGMP requirements
Reason cGMP Deviations; product does not comply with cGMP requirements
Reason Microbial Contamination of Non-Sterile Products: Lots failed microbiological testing at the 12-month time point.
Reason Marketed without an Approved NDA/ANDA; product is being manufactured and distributed without a NDC number
Reason Defective Delivery System; defective valve
Reason Failed Impurity/Degradation Specification; for 17-BMP at the 9 and 18 month stability time point
Reason Lack of Assurance of Sterility: All unexpired sterile compounded human and veterinary products are being recalled because they were compounded in the…
Reason Short Fill: Due to an error in the manufacturing process, cylinders in this lot may be empty and contain no medical oxygen.
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.