Complete FDA and NHTSA recall records dated in September 2017.
These records include useful source details for the selected month.
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to…
Presence of undeclared milk: the product lists butter as an ingredient but does not list milk as the source of the butter as required by FALCPA (Food Allergen Labeling and Consumer…
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to…
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to…
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to…
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to…
4-pack may contain banana nut muffin containing walnuts, allergen-walnuts not listed on the ingredient label
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to…
Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets
Marketed without an approved NDA/ANDA: presence of undeclared desmethyl carbodenafil and undeclared milk.
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Labeling Mixup; the individual A&D ointment foil packets are incorrectly labeled as petroleum jelly. The boxes and outer case are correctly labeled as A&D ointment.
Labeling: Not Elsewhere Classified; product is incorrectly labeled as Class III controlled substance instead of Class II controlled substance
Microbial contamination of Non-sterile Products; potential B. cepacia contamination
Marketed without an Approved NDA/ANDA;FDA analysis found product to be tainted with sildendafil and tadalafil
Microbial contamination of Non-sterile Products; potential B. cepacia contamination
Failed Impurities/Degradation Specification; out-of-specification results for individual unknown impurities at the 30 month Room Temperature Retained Sample stability test
PRESENCE OF FOREIGN TABLETS/CAPSULES: A 2.5 mg Amlodipine Besylate tablet was found co-mingled with 10 mg Amlodipine Besylate tablets in a bottle labeled as Amlodipine Besylate 10 mg.
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Products were manufactured from raw material (buttermilk solids) that may potentially be contaminated with Salmonella.
Products were manufactured from raw material (buttermilk solids) that may potentially be contaminated with Salmonella.
Madhava Natural Sweeteners is recalling MMM... Chocolate Chip Cookie Mix because it may contain undeclared milk.
Rushing Waters Fisheries is recalling 3 smoked fish products because they may have been underprocessed.
OPA by Litehouse Ranch was recalled due to undeclared egg.
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.
