FoodApr 12, 2017
Biery Cheese DIETZ & WATSON Pepper Jack Cheese NET WT recall — FDA F-1841-2017
The firm was notified by their supplier that various cheese products test positive for Listeria monocytogenes.
Class IFDA: TerminatedBiery Cheese, Inc.
April 2017 recalls — page 10
These records include useful source details for the selected month.
FoodApr 12, 2017
Biery Cheese DELALLO Premium Sliced HOT PEPPER CHEESE NET WT recall — FDA F-1839-2017
The firm was notified by their supplier that various cheese products test positive for Listeria monocytogenes.
Class IFDA: TerminatedBiery Cheese, Inc.
FoodApr 12, 2017
Ikea North America Srvcs Choklad Not recall — FDA F-1878-2017
IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%,…
Class IIFDA: TerminatedIkea North America Srvcs Inc.
FoodApr 12, 2017
Kwei Chow Sauce Industry Co net weight 7.40 Oz, sauce in glass jars, shelf stable recall — FDA F-1836-2017
Products contain undeclared wheat.
Class IIFDA: TerminatedKwei Chow Sauce Industry Co., Ltd.
FoodApr 12, 2017
Lipari Foods Thortons Italian & Provolone 12 oz recall — FDA F-1834-2017
JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
Class IFDA: TerminatedLipari Foods, Inc.
FoodApr 12, 2017
Lipari Foods Thortons Italian Footlong 6/12 oz recall — FDA F-1833-2017
JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.
Class IFDA: TerminatedLipari Foods, Inc.
FoodApr 12, 2017
Original Amish Bakery Schlabach Amish Bakery Chocolate Chip Grand-ola Bar NET WT recall — FDA F-1861-2017
The was notified that their label did not list "Soy" in the ingredient statement.
Class IIFDA: TerminatedOriginal Amish Bakery LLC
FoodApr 12, 2017
Biery Cheese Marketside Grab and Go Col Colby 10.8 oz Set Ups recall — FDA F-1846-2017
The firm was notified by their supplier that various cheese products test positive for Listeria monocytogenes.
Class IFDA: TerminatedBiery Cheese, Inc.
FoodApr 12, 2017
Kwei Chow Sauce Industry Co net weight 7.05 Oz, sauce in glass jars, shelf stable recall — FDA F-1837-2017
Products contain undeclared wheat.
Class IIFDA: TerminatedKwei Chow Sauce Industry Co., Ltd.
DrugApr 12, 2017
Ciclopirox Olamine Cream USP, 0.77% recall — FDA D-0636-2017
Labeling: Incorrect or Missing Package Insert: product lots packaged with an out-of-date insert.
Class IIIFDA: TerminatedG & W Laboratories, Inc.
DrugApr 12, 2017
SCA Pharmaceuticals Vancomycin HCl 1.25 g added to 5% Dextrose 250 mL Bag For IV Use Only recall — FDA D-0639-2017
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Class IFDA: TerminatedSCA Pharmaceuticals
DrugApr 12, 2017
SCA Pharmaceuticals Vancomycin HCl 1.5 gram added to 5% Dextrose 500 mL Total Approximate recall — FDA D-0643-2017
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Class IFDA: TerminatedSCA Pharmaceuticals
DrugApr 12, 2017
SCA Pharmaceuticals Vancomycin HCl 1 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use recall — FDA D-0640-2017
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Class IFDA: TerminatedSCA Pharmaceuticals
DrugApr 12, 2017
Hospira Inc., A Pfizer Company Vancomycin Hydrochloride for Injection, USP, 10 grams recall — FDA D-0638-2017
Presence of Particulate Matter: A hair was found stuck to the stopper of inside a single vial. The hair came in contact with the reconstituted drug product.
Class IFDA: TerminatedHospira Inc., A Pfizer Company
DrugApr 12, 2017
Organic Herbal Supply XtraHRD Natural Male Enhancement Capsules, Herbal Dietary Supplement recall — FDA D-0646-2017
Marketed without an Approved NDA/ANDA: Product contains N-desmethyl tadalafil an analogue to tadalafil which is an active pharmaceutical ingredient in a FDA approved drug used to treat…
Class IFDA: TerminatedOrganic Herbal Supply
DrugApr 12, 2017
RIVASTIGMINE Tartrate Capsules, USP, 1.5 mg, 60-count bottle recall — FDA D-0649-2017
Cross-contamination with other products -Related Substances test for Rivastigmine Tartrate Capsules USP, 1.5 mg showed a peak for Ranitidine.
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugApr 12, 2017
SCA Pharmaceuticals Vancomycin HCl 750 mg added to 5% Dextrose 250 mL For IV Use Only recall — FDA D-0645-2017
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Class IFDA: TerminatedSCA Pharmaceuticals
DrugApr 12, 2017
Ibuprofen Lysine Injection, 20 mg/2 mL (10 mg/mL), 2 mL Single-Dose Vial (NDC 39822-1030-1) recall — FDA D-0637-2017
Presence of Particulate Matter
Class IFDA: TerminatedX-Gen Pharmaceuticals Inc.
DrugApr 12, 2017
Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered recall — FDA D-0626-2017
Defective Delivery System: Elevated number of units with out of specification results for leak rate.
Class IIFDA: OngoingGlaxoSmithKline, LLC
DrugApr 12, 2017
Alvogen Adalat CC (nifedipine) Extended Release Tablets 30 mg, 100-count bottles recall — FDA D-0628-2017
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Class IIIFDA: TerminatedAlvogen, Inc.
DrugApr 12, 2017
SCA Pharmaceuticals Vancomycin HCl 1.5 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use recall — FDA D-0642-2017
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Class IFDA: TerminatedSCA Pharmaceuticals
DrugApr 12, 2017
SCA Pharmaceuticals Vancomycin HCl 1.25 g added to 0.9% Sodium Chloride 250 mL Bag For IV recall — FDA D-0641-2017
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Class IFDA: TerminatedSCA Pharmaceuticals
DrugApr 12, 2017
SCA Pharmaceuticals Vancomycin HCl 750 mg added to 250 mL 0.9% Sodium Chloride For IV Use recall — FDA D-0644-2017
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Class IFDA: TerminatedSCA Pharmaceuticals
FoodApr 5, 2017
Lipari Foods Copper wood Colby Jack Mini Horn, 4/6# recall — FDA F-1790-2017
Lipari Foods is recalling multiple cheeses because of a supplier's recall of cheese due to potential contamination with Listeria monocytogenes.
Class IFDA: TerminatedLipari Foods, Inc.
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.