FoodSep 27, 2017
Kilby Cream Birthday Cake Size: 7 oz recall — FDA F-3489-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
Monthly breakdown
2017 recalls by month
Select a month to review the recall records reported during that period.
December 2017112 records · 2 categoriesNovember 2017262 records · 2 categoriesOctober 201750 records · 2 categoriesSeptember 2017124 records · 2 categoriesAugust 2017178 records · 2 categoriesJuly 2017212 records · 2 categoriesJune 2017121 records · 3 categoriesMay 2017245 records · 3 categoriesApril 2017306 records · 2 categoriesMarch 2017226 records · 2 categoriesFebruary 2017106 records · 2 categoriesJanuary 2017396 records · 2 categories
2017 recalls — page 20
Records are ordered by the best available source date.
FoodSep 27, 2017
Kilby Cream Calfiene Size: Pint recall — FDA F-3493-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
FoodSep 27, 2017
Kilby Cream Ice Cream Various Flavors: Snickers Size: 2.5 Gal recall — FDA F-3548-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
FoodSep 27, 2017
SUNOPTA GRAINS AND FOODS Organic Great Value Dark Sweet Cherry Products Pitted, Net Wt recall — FDA F-3562-2017
Testing revealed the presence of Listeria monocytogenes in a finished product sample.
Class IFDA: TerminatedSUNOPTA GRAINS AND FOODS
FoodSep 27, 2017
Kilby Cream Ice Cream Various Flavors: S'mores Size: 2.5 Gal recall — FDA F-3547-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
FoodSep 27, 2017
The Coca-Cola Company Honest Kids Juice Slushy Blueberry Punch, 3.5-oz recall — FDA F-3561-2017
Due to a potential package design issue, there is the possibility for consumers to be injured when consuming the product from an unevenly opened pouch.
Class IIFDA: TerminatedThe Coca-Cola Company
FoodSep 27, 2017
Kilby Cream Black Raspberry Size: 7 oz recall — FDA F-3491-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
FoodSep 27, 2017
Kilby Cream Black Cherry Size: 7 oz recall — FDA F-3490-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
FoodSep 27, 2017
Kilby Cream Minty Moo Size: 2.5 Gal , 7 oz recall — FDA F-3508-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
FoodSep 27, 2017
Kilby Cream Island Breeze Size: 2.5 Gal recall — FDA F-3501-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
FoodSep 27, 2017
Kilby Cream Crow Vineyard Rose Size: 2.5 Gal recall — FDA F-3498-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
FoodSep 27, 2017
Kilby Cream Vanilla Size: 2.5 Gal , 7 oz recall — FDA F-3553-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
FoodSep 27, 2017
Kilby Cream 7 oz recall — FDA F-3550-2017
According to the firm a process deviation and proper temperatures were not reached during ice cream production and mix storage.
Class IIFDA: TerminatedKilby Cream
DrugSep 27, 2017
Procrit (epoetin alfa), 10,000 units/mL recall — FDA D-1173-2017
Presence of particulate matter: glass flakes identified as lamellae observed during a routine quality inspection.
Class IIFDA: TerminatedAmgen, Inc.
DrugSep 27, 2017
PharMedium Services Fentanyl Citrate (Preservative Free) 20 mcg per mL recall — FDA D-1166-2017
Labeling: Not Elsewhere Classified- Diluent used to compound product expired prior to the expiration date assigned to the compounded product.
Class IIFDA: TerminatedPharMedium Services, LLC
DrugSep 27, 2017
Levophed recall — FDA D-1168-2017
Lack of sterility assurance: resulting from use of a damaged sterilizing filter for nitrogen used in the manufacturing process.
Class IIFDA: TerminatedPfizer Inc.
DrugSep 27, 2017
HYDROmorphone HCl Injection, USP, 2 mg/mL, 1mL Single-use vial recall — FDA D-1167-2017
Lack of sterility assurance: resulting from use of a damaged sterilizing filter for nitrogen used in the manufacturing process.
Class IIFDA: TerminatedPfizer Inc.
DrugSep 27, 2017
Daytrana recall — FDA D-1169-2017
Defective Delivery System: Products no longer meet the release liner removal specification and/or z-statistic.
Class IIFDA: TerminatedNoven Pharmaceuticals, Inc.
DrugSep 27, 2017
Daytrana recall — FDA D-1172-2017
Defective Delivery System: Products no longer meet the release liner removal specification and/or z-statistic.
Class IIFDA: TerminatedNoven Pharmaceuticals, Inc.
DrugSep 27, 2017
Daytrana recall — FDA D-1170-2017
Defective Delivery System: Products no longer meet the release liner removal specification and/or z-statistic.
Class IIFDA: TerminatedNoven Pharmaceuticals, Inc.
DrugSep 27, 2017
Genentech Activase (alteplase), 100 mg (58 million IU), Lyophilized vial, packaged with 1 recall — FDA D-1175-2017
Non-Sterility:presence of cracked or chipped glass at the neck of Sterile Water for Injection vials.
Class IFDA: TerminatedGenentech, Inc.
DrugSep 27, 2017
PharMedium Services Fentanyl Citrate (Preservative Free) 10 mcg per mL recall — FDA D-1165-2017
Labeling: Not Elsewhere Classified- Diluent used to compound product expired prior to the expiration date assigned to the compounded product.
Class IIFDA: TerminatedPharMedium Services, LLC
DrugSep 27, 2017
Daytrana recall — FDA D-1171-2017
Defective Delivery System: Products no longer meet the release liner removal specification and/or z-statistic.
Class IIFDA: TerminatedNoven Pharmaceuticals, Inc.
DrugSep 27, 2017
Medisca Aminocaproic Acid, USP (6-Aminohexanoic Acid) active pharmaceutical ingredient recall — FDA D-1174-2017
CGMP Deviations: Product manufactured for Industrial Use but was labeled and distributed for Pharmacy Compounding Use.
Class IIFDA: TerminatedMedisca, Inc.
About the 2017 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.