FoodAug 6, 2014
PUREFRUIT CHILE S.A fruty U applesauce, apple recall — FDA F-2230-2014
Purefruit Chile S.A. is recalling pouched applesauce due to the possibility of mold.
Class IIFDA: TerminatedPUREFRUIT CHILE S.A
August 2014 recalls — page 5
These records include useful source details for the selected month.
FoodAug 6, 2014
Richard's Rub & Seasonings Richards Too Good BBQ Sauce recall — FDA F-2233-2014
Richards Rubs & Seasonings LLC is recalling Richards Too Good BBQ Sauce, Richards Too Good Hot Sauce and Richards Too Good Teriyaki Sauce because they may have been improperly processed and…
Class IIFDA: TerminatedRichard's Rub & Seasonings, LLC
FoodAug 6, 2014
Richard's Rub & Seasonings Richards Too Good Teriyaki Sauce recall — FDA F-2235-2014
Richards Rubs & Seasonings LLC is recalling Richards Too Good BBQ Sauce, Richards Too Good Hot Sauce and Richards Too Good Teriyaki Sauce because they may have been improperly processed…
Class IIFDA: TerminatedRichard's Rub & Seasonings, LLC
FoodAug 6, 2014
PUREFRUIT CHILE S.A HyVee applesauce recall — FDA F-2232-2014
Purefruit Chile S.A. is recalling pouched applesauce due to the possibility of mold.
Class IIFDA: TerminatedPUREFRUIT CHILE S.A
DrugAug 6, 2014
Dermamedics Calm and Correct Serum, 2 oz. containers with a SKU number of BB10062 and 4 oz. recall — FDA D-1491-2014
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
Class IIFDA: TerminatedDermamedics, LLC
DrugAug 6, 2014
Daiichi Sankyo Pharma Development Azor Tablets recall — FDA D-1501-2014
Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping
Class IIFDA: TerminatedDaiichi Sankyo Pharma Development
DrugAug 6, 2014
Daiichi Sankyo Pharma Development Benicar Tablets (olmesartan medoxomil) 40 mg, 30 and 90 recall — FDA D-1506-2014
Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping.
Class IIFDA: TerminatedDaiichi Sankyo Pharma Development
DrugAug 6, 2014
Pfizer Cardura XL recall — FDA D-1485-2014
Failed Impurities/Degradation Specifications: Product from this lot may not meet specifications for a product degradant.
Class IIIFDA: TerminatedPfizer Inc.
DrugAug 6, 2014
Daiichi Sankyo Pharma Development Benicar Tablets (olmesartan medoxomil) 20 mg, 30 and 90 recall — FDA D-1502-2014
Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping
Class IIFDA: TerminatedDaiichi Sankyo Pharma Development
DrugAug 6, 2014
Daiichi Sankyo Pharma Development Tribenzor Tablets recall — FDA D-1504-2014
Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping
Class IIFDA: TerminatedDaiichi Sankyo Pharma Development
DrugAug 6, 2014
Dermamedics Complexion Repair Topical Rehydrating Emulsion in 50 ml and 30 ml containers in recall — FDA D-1494-2014
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
Class IIFDA: TerminatedDermamedics, LLC
DrugAug 6, 2014
Daiichi Sankyo Pharma Development Benicar HCT Tablets recall — FDA D-1508-2014
Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping.
Class IIFDA: TerminatedDaiichi Sankyo Pharma Development
DrugAug 6, 2014
Fagron recall — FDA D-1497-2014
Microbial Contamination of Non-Sterile Products: Fagron is recalling six lots due to the presence of mold.
Class IIFDA: TerminatedFagron, Inc.
DrugAug 6, 2014
Daiichi Sankyo Pharma Development Benicar HCT Tablets recall — FDA D-1503-2014
Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping
Class IIFDA: TerminatedDaiichi Sankyo Pharma Development
DrugAug 6, 2014
Dermamedics Therametics Complexion Repair Topical Rehydrating Emulsion in 50 ml and 30 ml recall — FDA D-1495-2014
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
Class IIFDA: TerminatedDermamedics, LLC
DrugAug 6, 2014
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle recall — FDA D-1500-2014
Presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel.
Class IIFDA: TerminatedJubilant Cadista Pharmaceuticals Inc.
DrugAug 6, 2014
Dermamedics Baby's Relief Calm and Repair Cream in 2 oz. containers with a SKU number of recall — FDA D-1489-2014
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
Class IIFDA: TerminatedDermamedics, LLC
DrugAug 6, 2014
Daiichi Sankyo Pharma Development Benicar HCT Tablets recall — FDA D-1507-2014
Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping.
Class IIFDA: TerminatedDaiichi Sankyo Pharma Development
DrugAug 6, 2014
Dermamedics Complexion Repair Topical Rehydrating Emulsion which was recall — FDA D-1490-2014
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
Class IIFDA: TerminatedDermamedics, LLC
DrugAug 6, 2014
Fagron recall — FDA D-1498-2014
Microbial Contamination of Non-Sterile Products: Fagron is recalling six lots due to the presence of mold.
Class IIFDA: TerminatedFagron, Inc.
DrugAug 6, 2014
Fagron recall — FDA D-1496-2014
Microbial Contamination of Non-Sterile Products: Fagron is recalling six lots due to the presence of mold.
Class IIFDA: TerminatedFagron, Inc.
DrugAug 6, 2014
Teva Pharmaceuticals USA triple therapy, LANSOPRAZOLE DR Capsules USP 30mg, CLARITHROMYCIN recall — FDA D-1499-2014
Failed Impurities/Degradation Specifications: This recall is due to out of specification for impurities test results obtained during stability testing for Lansoprazole.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
How to use this monthly recall archive
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.