DrugJun 7, 2017
SCA Pharmaceuticals morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total recall — FDA D-0871-2017
Lack of assurance of sterility: Product bags leaking at seam.
Class IIFDA: TerminatedSCA Pharmaceuticals
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 45
Records are ordered by the best available source date.
DrugJun 7, 2017
SCA Pharmaceuticals HYDROmorphone HCL in 0.9% Sodium Chloride injectable, 0.2 mg per ml recall — FDA D-0875-2017
Lack of assurance of sterility: Product bags leaking at seam.
Class IIFDA: TerminatedSCA Pharmaceuticals
DrugJun 7, 2017
SCA Pharmaceuticals ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 2g recall — FDA D-0876-2017
Lack of assurance of sterility: Product bags leaking at seam.
Class IIFDA: TerminatedSCA Pharmaceuticals
FoodMay 31, 2017
Italian Gluten Free Foods CL 15 oz recall — FDA F-2246-2017
Product contains undeclared eggs
Class IFDA: TerminatedItalian Gluten Free Foods CL
FoodMay 31, 2017
Reel Fresh UPC: 664183001454 Ingredients: Frozen tuna and carbon monoxide recall — FDA F-2268-2017
Frozen raw tuna cubes from Indonesia tested positive for hepatitis A.
Class IFDA: TerminatedTropic Fish Hawaii, LLC
FoodMay 31, 2017
Lords Organics Organic Veda brand Ginger Powder, 24 jars, Net Wt recall — FDA F-2236-2017
Lord Organics is recalling ginger powder because it has the potential to be contaminated with Salmonella.
Class IFDA: TerminatedLords Organics LLC
FoodMay 31, 2017
Rich Products ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following recall — FDA F-2242-2017
The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.
Class IIFDA: TerminatedRich Products Corp
FoodMay 31, 2017
U S Deer Antlers Export & Import 40 pouches/case recall — FDA F-2249-2017
US Deer Antler Export and Import is recalling a variety of Herbal Teas because they may be contaminated with Clostridium botulinum
Class IFDA: TerminatedU S Deer Antlers Export & Import
FoodMay 31, 2017
Phoenix Food Dip Trio Mix Homemade Gourmet Dip Mix Net Wt recall — FDA F-2245-2017
Possible Salmonella contamination.
Class IFDA: TerminatedPhoenix Food, LLC
FoodMay 31, 2017
RB Manufacturing Schiff Move Free Advanced Plus MSM & Vitamin D3 with recall — FDA F-2250-2017
RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.
Class IIIFDA: TerminatedRB Manufacturing LLC
FoodMay 31, 2017
Rich Products ARTISAN CRUST PIZZA DOUGH 24/18, PRODUCT CODE 11413, UPC 1 00 recall — FDA F-2244-2017
The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.
Class IIFDA: TerminatedRich Products Corp
FoodMay 31, 2017
Rich Products 7 OZ PIZZA DOUGH BALL, PRODUCT CODE 11267, UPC 0 00 49800 1267 recall — FDA F-2243-2017
The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.
Class IIFDA: TerminatedRich Products Corp
FoodMay 31, 2017
SK Food Group Groveport Slow Roasted Ham & Swiss Breakfast Sandwich, Fully Cooked/Keep recall — FDA F-2241-2017
The product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedSK Food Group Groveport
DrugMay 31, 2017
Standard Homeopathic Company Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS recall — FDA D-0864-2017
Superpotent Drug: FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the product labels.
Class IFDA: TerminatedStandard Homeopathic Company
DrugMay 31, 2017
Ventolin HFA (albuterol sulfate) Inhalation, 90 mcg per actuation, 200 Metered Inhalations recall — FDA D-0793-2017
Defective Delivery System: Elevated number of units with out of specification results for leak rate
Class IIFDA: OngoingGlaxoSmithKline, LLC
DrugMay 31, 2017
SATO CLEAR recall — FDA D-0855-2017
Lack of Assurance of Sterility: Firm failed to establish an adequate system for monitoring environmental conditions in aseptic processing areas.
Class IIFDA: TerminatedSato Pharmaceutical Inc.
DrugMay 31, 2017
Sato Pharmaceutical DORAMA-NEO recall — FDA D-0856-2017
Lack of Assurance of Sterility: Firm failed to establish an adequate system for monitoring environmental conditions in aseptic processing areas.
Class IIFDA: TerminatedSato Pharmaceutical Inc.
DrugMay 31, 2017
Sun Pharmaceutical Industries Children's Cetirizine Hydrochloride Chewable Tablets, 5 mg recall — FDA D-0857-2017
Failed Tablet/Capsule Specifications: out of specification results for increased tablet hardness.
Class IIIFDA: TerminatedSun Pharmaceutical Industries, Inc.
DrugMay 31, 2017
Fagron Estriol, For Prescription Compounding recall — FDA D-0791-2017
cGMP Deviations: lack of quality assurance at the API manufacturer.
Class IIFDA: TerminatedFagron, Inc.
DrugMay 31, 2017
Mylan Pharmaceuticals Tarina Fe 1/20 recall — FDA D-0860-2017
Chemical Contamination: out of specification results for impurities were found to be the result of contamination of product from vapors associated with paint thinner used in repair of the…
Class IIIFDA: TerminatedMylan Pharmaceuticals Inc.
DrugMay 31, 2017
Sato Pharmaceutical Optic Splash recall — FDA D-0854-2017
Lack of Assurance of Sterility: Firm failed to establish an adequate system for monitoring environmental conditions in aseptic processing areas.
Class IIFDA: TerminatedSato Pharmaceutical Inc.
DrugMay 31, 2017
Cell Distributors Refresh Tears recall — FDA D-0865-2017
Labeling: Not elsewhere classified; product labeling lacks a NDC number, net weight information and does not contain the Drug Facts Panel.
Class IIFDA: TerminatedCell Distributors
DrugMay 31, 2017
DEXTROSE Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use recall — FDA D-0862-2017
Presence of Particulate Matter: human hair found within an internal sample syringe.
Class IFDA: OngoingHospira Inc.
DrugMay 31, 2017
Standard Homeopathic Company Hyland's Baby Teething Tablets [Calcarea Phosporica 6X HPUS recall — FDA D-0863-2017
Superpotent Drug: FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the product labels.
Class IFDA: TerminatedStandard Homeopathic Company
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.