DrugMay 25, 2016
Keystone Laboratories BETTER BRAIDS UN-BRAID (salicylic acid), Le Demelant recall — FDA D-0853-2016
Microbial Contamination of Non-Sterile Products: Failed S.aureus test.
Class IIFDA: TerminatedKeystone Laboratories Inc.
Monthly breakdown
2016 recalls by month
Select a month to review the recall records reported during that period.
December 2016251 records · 2 categoriesNovember 2016140 records · 2 categoriesOctober 2016469 records · 2 categoriesSeptember 2016304 records · 3 categoriesAugust 2016156 records · 3 categoriesJuly 2016295 records · 2 categoriesJune 2016155 records · 2 categoriesMay 2016210 records · 2 categoriesApril 2016193 records · 2 categoriesMarch 2016166 records · 2 categoriesFebruary 2016176 records · 2 categoriesJanuary 201693 records · 2 categories
2016 recalls — page 76
Records are ordered by the best available source date.
DrugMay 25, 2016
Allegiant Health col-rite (docusate sodium) stool softener softgels, 50 mg recall — FDA D-0856-2016
Superpotent Drug: High out of specification results for assay at the 6 month time point interval.
Class IIIFDA: TerminatedAllegiant Health
FoodMay 18, 2016
Garden Of Life Raw Meal Organic Chocolate Powder recall — FDA F-1328-2016
Products possibly contaminated with Salmonella
Class IFDA: TerminatedGarden Of Life LLC
FoodMay 18, 2016
Salsa Dianne Lemon Pesto Sauce, net wt recall — FDA F-1323-2016
Lemon Pesto Sauce recalled because parmesan cheese is declared but milk is not declared on label.
Class IIFDA: TerminatedSalsa Dianne
FoodMay 18, 2016
Greater Pittsburgh Community Food Bank Imperial Choice Mandarin Oranges Broken Segments in recall — FDA F-1245-2016
Greater Pittsburgh Community Food Bank is announcing a voluntary recall of one lot of Imperial Choice Mandarin Oranges Broken Segments in Light Syrup because some of the cans from this lot…
Class IIIFDA: TerminatedGreater Pittsburgh Community Food Bank
FoodMay 18, 2016
Bertagni 1882 Meijer frozen Butternut Squash Ravioli, product is packaged in recall — FDA F-1044-2016
Meijer frozen Butternut Squash Ravioli is recalled because product may contain undeclared cashew and almond.
Class IFDA: TerminatedBertagni 1882
FoodMay 18, 2016
Bertagni 1882 packaged in a paper tray inside a plastic bag and wrapped recall — FDA F-1043-2016
Bertagni fresh Sweet Butternut Squash Ravioli is recalled because the products may contain undeclared cashew and almond.
Class IFDA: TerminatedBertagni 1882
FoodMay 18, 2016
Salsa Dianne Classic Pesto Sauce recall — FDA F-1322-2016
Classic Pesto Sauce (with a twist) is recalled because Parmesan cheese is declared but milk is not declared on label.
Class IIFDA: TerminatedSalsa Dianne
FoodMay 18, 2016
Garden Of Life Raw Meal Organic Original Powder recall — FDA F-1329-2016
Products possibly contaminated with Salmonella
Class IFDA: TerminatedGarden Of Life LLC
FoodMay 18, 2016
Garden Of Life Raw Meal Organic Vanilla Powder recall — FDA F-1327-2016
Products possibly contaminated with Salmonella
Class IFDA: TerminatedGarden Of Life LLC
FoodMay 18, 2016
Nuwati Herbals SeeLessO'Me Diet and Weight Management Tea recall — FDA F-1331-2016
Product contains undeclared soy.
Class IIFDA: TerminatedNuwati Herbals Inc.
FoodMay 18, 2016
Garden Of Life Raw Meal Organic Vanilla Spiced Chai Powder recall — FDA F-1330-2016
Products possibly contaminated with Salmonella
Class IFDA: TerminatedGarden Of Life LLC
DrugMay 18, 2016
Sesderma, SL Dryses Aluminum Chlorohydrate Deodorant for Women, Roll-on, 2.5 fl oz (75 mL) recall — FDA D-0847-2016
cGMP Deviations; product does not comply with cGMP requirements
Class IIFDA: OngoingSesderma, SL
DrugMay 18, 2016
Sesderma, SL Repaskin 30 recall — FDA D-0849-2016
cGMP Deviations; product does not comply with cGMP requirements
Class IIFDA: OngoingSesderma, SL
DrugMay 18, 2016
Sesderma, SL Screenses Color Sunscreen Tinted facial make-up compact, Broad Spectrum SPF 50 recall — FDA D-0850-2016
cGMP Deviations; product does not comply with cGMP requirements
Class IIFDA: OngoingSesderma, SL
DrugMay 18, 2016
Sesderma, SL Repaskin 30 recall — FDA D-0845-2016
cGMP Deviations; product does not comply with cGMP requirements
Class IIFDA: OngoingSesderma, SL
DrugMay 18, 2016
Sesderma, SL Salises Facial Moisturizing Acne Treatment Gel, (salicylic acid 1.5%), 1.7 fl. recall — FDA D-0843-2016
cGMP Deviations; product does not comply with cGMP requirements
Class IIFDA: OngoingSesderma, SL
DrugMay 18, 2016
Sesderma, SL Repaskin 50 recall — FDA D-0848-2016
cGMP Deviations; product does not comply with cGMP requirements
Class IIFDA: OngoingSesderma, SL
DrugMay 18, 2016
Sesderma, SL Dryses Aluminum Chlorohydrate Deodorant for Men Roll-on, 2.5 fl oz (75 mL) recall — FDA D-0846-2016
cGMP Deviations; product does not comply with cGMP requirements
Class IIFDA: OngoingSesderma, SL
DrugMay 18, 2016
Sesderma, SL Repaskin 50 recall — FDA D-0844-2016
cGMP Deviations; product does not comply with cGMP requirements
Class IIFDA: OngoingSesderma, SL
DrugMay 18, 2016
Sesderma, SL Dryses Aluminum Chlorohydrate Antiperspirant Solution, 3.4 fl. oz (100 mL) recall — FDA D-0842-2016
cGMP Deviations; product does not comply with cGMP requirements
Class IIFDA: OngoingSesderma, SL
DrugMay 18, 2016
Sesderma, SL Screenses Color Sunscreen, Tinted facial make-up compact, Broad Spectrum SPF 50 recall — FDA D-0851-2016
cGMP Deviations; product does not comply with cGMP requirements
Class IIFDA: OngoingSesderma, SL
FoodMay 11, 2016
Iowa Select Herbs Dandelion Leaf recall — FDA F-1168-2016
Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary…
Class IIIFDA: TerminatedIowa Select Herbs LLC
FoodMay 11, 2016
R.W. Bakers Co Assorted Dinner Rolls, 128 ct., Net Wt recall — FDA F-1307-2016
R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer Plain Knot Rolls" and 8 ct. packages of Assorted Dinner Rolls 128 ct. because they may contain trace amounts of…
Class IIFDA: TerminatedR.W. Bakers Co. Inc.
About the 2016 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.