FoodJan 19, 2022
NutraCap Labs Hi-T Level Up Capsules 120ct Bottle UPC CODE recall — FDA F-0447-2022
During an FDA investigation the firm was notified that the product contains undeclared milk.
Class IFDA: TerminatedNutraCap Labs LLC
Latest records
Latest recalls — page 783
The newest recall records with useful source details are listed here.
FoodJan 19, 2022
Maryland & Virginia Milk Producers butter almond HOWLING COW THE ICE CREAM OF NC STATE recall — FDA F-0366-2022
The firm was notified by a customer that the Butter Almond containers contains Cookie Dough Ice Cream. The Cookie Dough Ice Cream contains soy and wheat which are not listed on the label…
Class IFDA: TerminatedMaryland & Virginia Milk Producers
FoodJan 19, 2022
NutraCap Labs Huge Nutrition Enhance Capsules 240ct Bottle UPC CODE 7 28614 recall — FDA F-0449-2022
During an FDA investigation the firm was notified that the product contains undeclared milk.
Class IFDA: TerminatedNutraCap Labs LLC
FoodJan 19, 2022
Local Fixe Fresh Flour Tortillas are packaged in a clear Ziploc style recall — FDA F-0388-2022
Flour is declared but Wheat is not declared on label.
Class IIFDA: TerminatedLocal Fixe LLC
FoodJan 19, 2022
Lidl US Operations Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7 fl recall — FDA F-0394-2022
Undeclared milk allergen
Class IIFDA: TerminatedLidl US Operations, LLC
FoodJan 19, 2022
NutraCap Labs OTAK Innovations OTAK:AM Capsules 90ct Bottle UPC CODE 4 08012 recall — FDA F-0474-2022
During an FDA investigation the firm was notified that the product contains undeclared milk.
Class IFDA: TerminatedNutraCap Labs LLC
FoodJan 19, 2022
NutraCap Labs BlakeFit Everyday All-in-one Lime Watermelon 44oz Jar UPC CODE recall — FDA F-0419-2022
During an FDA investigation the firm was notified that the product contains undeclared milk.
Class IFDA: TerminatedNutraCap Labs LLC
DrugJan 19, 2022
Metoprolol Tartrate Tablets, USP 25 mg, 1000 - count bottle recall — FDA D-0362-2022
Complaint received of foreign matter (metal) embedded in tablet.
Class IIFDA: TerminatedRubicon Research Private Limited
DrugJan 19, 2022
Teva Pharmaceuticals USA Norepinephrine Bitartrate Injection USP 4 mg/4 mL (1 mg/mL), 4 mL recall — FDA D-0371-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugJan 19, 2022
Akorn Sufentanil Citrate Injection, USP 100 mcg/2 mL (50 mcg/mL) for intravenous and recall — FDA D-0460-2022
Subpotent Drug: Out of specification for assay at the 30-month stability timepoint.
Class IIFDA: TerminatedAkorn, Inc.
DrugJan 19, 2022
Revive Personal Products Company The Natural Dentist Healthy Balance Peppermint Sage recall — FDA D-0364-2022
Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Menthol with UPC 7 14132 00071 4 instead of Peppermint Oil and Sage Oil with UPC 7 14132 00073 8
Class IIFDA: OngoingRevive Personal Products Company
DrugJan 19, 2022
Teva Pharmaceuticals USA MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL recall — FDA D-0370-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugJan 19, 2022
Clobetasol Propionate Ointment USP, 0.05%, 60g tubes recall — FDA D-0375-2022
Microbial Contamination of Non-Sterile Products: presence of R. Pickettii bacteria
Class IFDA: TerminatedTaro Pharmaceuticals U.S.A., Inc.
DrugJan 19, 2022
Nitroglycerin Lingual Spray, 400 mcg per spray, 200 metered sprays, 12 g bottles recall — FDA D-0372-2022
Defective Delivery System
Class IIFDA: TerminatedPadagis US LLC
Medical DeviceJan 12, 2022
DiaSorin Molecular Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455 recall — FDA Z-0457-2022
A subset of affected discs are at risk of leakage when it is used more than one time with Simplexa COVID-19 Direct and/or Simplexa Flu A/B & RSV Direct Gen II. Leakage from a well that had…
Class IIFDA: OngoingDiaSorin Molecular LLC
Medical DeviceJan 12, 2022
CRHF Instructions for Use for all model numbers of the Medtronic Abre Venous Self-Expanding recall — FDA Z-0464-2022
There have been reports of stent migration.
Class IIFDA: TerminatedMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJan 12, 2022
Siemens Healthcare Diagnostics Atellica CH 930 Analyzer with Software version: V1.25.1 and recall — FDA Z-0449-2022
(1)Software (SW) versions V1.25.1 and lower may result in TDef (Test Definition) Parameters for Open Channel Assays reverting to Default Value would shift test results by the magnitude of…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceJan 12, 2022
Flower Orthopedics Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to recall — FDA Z-0448-2022
Mating incompatibility between the Inserter Shaft and the Inserter Draw Rod causing the inserter draw rod to bind and not rotate freely as intended surgeon may be unable to complete surgery…
Class IIFDA: TerminatedFlower Orthopedics Corporation
Medical DeviceJan 12, 2022
Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair recall — FDA Z-0447-2022
Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the…
Class IIFDA: OngoingInvacare Corporation
Medical DeviceJan 12, 2022
Abbott Molecular Alinity m System, Part No. 08N53-002 recall — FDA Z-0463-2022
There is an issue with the installation of updated camera firmware on the system.
Class IIFDA: TerminatedAbbott Molecular, Inc.
Medical DeviceJan 12, 2022
Invacare TDX SP2 with LiNX Gyro Power Wheelchair recall — FDA Z-0445-2022
Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the…
Class IIFDA: OngoingInvacare Corporation
Medical DeviceJan 12, 2022
Abbott Molecular Alinity m System, Part No. 08N53-002 recall — FDA Z-0462-2022
There is a software defect that can cause the Amplification Detection clamp CLEAN position to be set too high.
Class IIFDA: TerminatedAbbott Molecular, Inc.
Medical DeviceJan 12, 2022
Abbott Molecular Alinity m System, Part No. 08N53-002 recall — FDA Z-0461-2022
There is a software issue associated with the ability to properly complete a Field Service Engineer Maintenance and Diagnostics procedure.
Class IIFDA: OngoingAbbott Molecular, Inc.
Medical DeviceJan 12, 2022
Tapemark Company iontoPATCH On-the-Go Patch Therapy, Transdermal Iontophoretic Drug Delivery recall — FDA Z-0454-2022
The dosage information on the pouch is incorrect; the primary carton label is correct.
Class IIIFDA: TerminatedTapemark Company
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 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