FoodDec 21, 2016
First Source Flave! TROPICAL TRAIL MIX, NET WT 8OZ recall — FDA F-0699-2017
Product has the potential to be contaminated with Listeria monocytogenes
Class IFDA: TerminatedFirst Source LLC
December 2016 recalls — page 7
These records include useful source details for the selected month.
DrugDec 21, 2016
Cantrell Drug Company Calcium Chloride 1 g/50 mL* Added to 5% Dextrose (20 mg/mL)* recall — FDA D-0184-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Morphine Sulfate 1 mg/mL in 0.9% Sodium Chloride, 100 mL Bag recall — FDA D-0199-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Phenylephrine HCl 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 recall — FDA D-0185-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride 30 mL PCA Vial recall — FDA D-0196-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Midazolam HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) recall — FDA D-0198-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Fentanyl Citrate 2 mcg/mL & Bupivacaine HCl 0.125% in 0.9% Sodium recall — FDA D-0190-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Rocuronium Bromide 50 mg/5 mL Injection Solution, 5 mL (10 mg/mL) recall — FDA D-0202-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Neostigmine Methylsulfate 5 mg/5 mL Injection Solution, 5 mL (1 mg/mL) recall — FDA D-0200-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Glycopyrrolate 1 mg/5 mL (0.2 mg/mL) Injection Solution, 5 mL recall — FDA D-0191-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Heparin Sodium 5,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL* recall — FDA D-0193-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag recall — FDA D-0186-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL recall — FDA D-0204-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Ropivacaine HCl 0.25% in 0.9% Sodium Chloride, 100 mL Bag, Epidural recall — FDA D-0203-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 mg/mL) recall — FDA D-0194-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 150 mL recall — FDA D-0188-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Jubilant Cadista Pharmaceuticals Methylprednisolone Tablets, USP, 16 mg, 50-count bottles recall — FDA D-0205-2017
Labeling: Incorrect or Missing Lot and/or Exp Date: incorrect expiration date of 02/0218 is printed on the container label instead of the correct expiration date of 02/2018.
Class IIIFDA: TerminatedJubilant Cadista Pharmaceuticals, Inc.
DrugDec 21, 2016
Cantrell Drug Company Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium recall — FDA D-0192-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Fentanyl Citrate 2,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 250 mL* recall — FDA D-0189-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) recall — FDA D-0195-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
DrugDec 21, 2016
Cantrell Drug Company Oxytocin 30 USP Units Added to 0.9% Sodium Chloride, 500 mL Bag recall — FDA D-0201-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class IIFDA: TerminatedCantrell Drug Company
FoodDec 14, 2016
OLMA-XXI SALMON, TURBOT, BUTTERFISH, smoked sliced, Net Weight: 8oz recall — FDA F-0598-2017
Products have the potential to be contaminated with Listeria monocytogenes
Class IFDA: TerminatedOLMA-XXI Inc.
FoodDec 14, 2016
Chocolate Shoppe Ice Cream Co Peanut Butter Cookie Dough Ice Cream, 3 gallons recall — FDA F-0573-2017
The Chocolate Chip Cookie Dough pieces in the ice cream have the potential to be contaminated with Listeria monocytogenes. EXPANDED 11/10/2016 Recall has been expanded after being notified…
Class IFDA: TerminatedChocolate Shoppe Ice Cream Co., Inc.
FoodDec 14, 2016
Club Chef in 7.625 lb cases, containing 1bag recall — FDA F-0589-2017
The firm was notified by their supplier that the product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedClub Chef LLC
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.