Phentermine Hydrochloride Capsules, USP, 15 mg recall — FDA D-0574-2016
Failed impurities/Degradation specifications: out of specification results for individual unknown and total impurity at the 12th month room temperature stability test station
Complete FDA and NHTSA recall records dated in January 2016.
These records include useful source details for the selected month.
Failed impurities/Degradation specifications: out of specification results for individual unknown and total impurity at the 12th month room temperature stability test station
Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count
Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count
Presence of particulate matter: Presence of silicone oil microdroplets in bevacizumab syringes for intravitreal use.
Presence of particulate matter: Presence of silicone oil microdroplets in bevacizumab syringes for intravitreal use.
Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count
Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count
Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count
Presence of particulate matter: Presence of silicone oil microdroplets in bevacizumab syringes for intravitreal use.
Presence of foreign substance -This recall has been intiated due to the presence of a polyethylene piece on the finished product.
Microbial Contamination of Non Sterile Products; testing revealed out of specification results for total aerobic microbiological count
Presence of particulate matter: Presence of silicone oil microdroplets in bevacizumab syringes for intravitreal use.
Presence of Foreign Substance
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
The firm was manufacturing acidified foods without a license.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.