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.
Latest records
Latest recalls — page 1662
The newest recall records with useful source details are listed here.
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Labeling: Incorrect or Missing Package Insert: product lots packaged with an out-of-date insert.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
Medical DeviceApr 5, 2017
Resource Optimization & Innovation Regard, Item Number: 800558001, Sterile, OR0647A recall — FDA Z-1621-2017
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Class IIFDA: TerminatedResource Optimization & Innovation LLC
Medical DeviceApr 5, 2017
Resource Optimization & Innovation Regard, Item Number: 800524002, Sterile, LD0608B - C recall — FDA Z-1588-2017
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Class IIFDA: TerminatedResource Optimization & Innovation LLC
Medical DeviceApr 5, 2017
Focus Diagnostics Legionella IFA (IF0950) intended for qualitatively detecting and recall — FDA Z-1685-2017
After a submission for CLIA database update from Focus Diagnostics to DiaSorin Molecular,the company found that their Legionella IFA device (IF0950) is not 510(k) exempt.
Class IIFDA: TerminatedFocus Diagnostics Inc.
Medical DeviceApr 5, 2017
Resource Optimization & Innovation Regard, Item Number: 800546001 Sterile, GS0635A recall — FDA Z-1604-2017
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Class IIFDA: TerminatedResource Optimization & Innovation LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026245 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026371 records · 4 categoriesJune 2026375 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories