FoodMay 16, 2018
STONEWALL KITCHEN Basil Pesto Aioli Net Weight Net 10.25 oz recall — FDA F-1440-2018
Product may contain undeclared eggs.
Class IFDA: TerminatedStonewall Kitchen, LLC
Monthly breakdown
2018 recalls by month
Select a month to review the recall records reported during that period.
December 2018285 records · 4 categoriesNovember 2018342 records · 4 categoriesOctober 2018626 records · 4 categoriesSeptember 2018393 records · 4 categoriesAugust 2018569 records · 4 categoriesJuly 2018356 records · 4 categoriesJune 2018402 records · 4 categoriesMay 2018613 records · 4 categoriesApril 2018449 records · 3 categoriesMarch 2018523 records · 3 categoriesFebruary 2018612 records · 3 categoriesJanuary 2018290 records · 3 categories
2018 recalls — page 142
Records are ordered by the best available source date.
FoodMay 16, 2018
Bob's Red Mill Natural Foods Item 1674C194, packaged in flexible packaging bag, 4 bags to a recall — FDA F-1389-2018
100% Whole Wheat Bread Mix is recalled due to undeclared wheat in the label on the back side of the package.
Class IIFDA: TerminatedBob's Red Mill Natural Foods, Inc.
FoodMay 16, 2018
Greenbelt Greenhouse Sunflower Microgreens, Greenbelt Microgreens brand, net wt recall — FDA F-1472-2018
Sunflower Microgreens product is recalled due to a potential to be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedGreenbelt Greenhouse Ltd
FoodMay 16, 2018
TRIANGLE PHARMANATURALS Lifted Kratom Red Maeng Da in 45 gram powder, 150 capsule and recall — FDA F-1431-2018
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Class IFDA: TerminatedTRIANGLE PHARMANATURALS LLC
FoodMay 16, 2018
Superior Foods Company Smoked Salmon Spread 5 lb recall — FDA F-1390-2018
Superior Foods Company is voluntarily recalling a specific lot of Smoked Salmon Spreads that were produced on March 26, 2018, due to potential contamination with Listeria monocytogenes.
Class IFDA: TerminatedSuperior Foods Company
FoodMay 16, 2018
Eastland Food Asian Best, Tamarind Candy Hot Flavor Net Weight: 4 oz recall — FDA F-1408-2018
Eastland Food Corporation out an abundance of caution has decided to initiate a product recall of all Asian Best, Tamarind Candy ( UPC: 083737158008 ) and Tamarind Candy Hot Flavor ( UPC:…
Class IIFDA: TerminatedEastland Food Corporation
FoodMay 16, 2018
Greenbelt Greenhouse Spicy Microgreen Mix, Greenbelt Microgreens brand, net wt recall — FDA F-1470-2018
Spicy Microgreen Mix product is recalled due to a potential to be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedGreenbelt Greenhouse Ltd
FoodMay 16, 2018
TRIANGLE PHARMANATURALS Lifted Kratom Green Maeng Da in 45 gram powder, 150 capsule recall — FDA F-1432-2018
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Class IFDA: TerminatedTRIANGLE PHARMANATURALS LLC
FoodMay 16, 2018
Greenbelt Greenhouse Fresh Microgreen Mix, Greenbelt Microgreens brand, net wt recall — FDA F-1468-2018
Fresh Microgreen Mix product is recalled due to a potential to be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedGreenbelt Greenhouse Ltd
DrugMay 16, 2018
Vitalab Pharmacy Alprostadil 20 mcg/mL, Sterile injectable, Vitalab Pharmacy, Inc recall — FDA D-0729-2018
Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns may not be sufficient to support the…
Class IIFDA: TerminatedVitalab Pharmacy, Inc.
DrugMay 16, 2018
Ampicillin and Sulbactam for Injection, USP, 3 gram*s/vial, For Intramuscular or Intravenous recall — FDA D-0866-2018
Presence of Particulate Matter: confirmed customer report of the presence of visible particulate matter believed to be red rubber particles from the manufacturing process of the active…
Class IFDA: TerminatedAuroMedics Pharma LLC
DrugMay 16, 2018
OraVerse (Phentolamine Mesylate) Injection, 0.4 mg/1.7mL recall — FDA D-0828-2018
Failed Impurities/Degradation: This recall has been initiated due to an out of specification (OOS) result that was obtained for related substance (Phentolamide), a known degradation product…
Class IIIFDA: TerminatedSeptodont Inc.
DrugMay 16, 2018
Vitalab Pharmacy Papaverine 30mg/Phentolamine 2mg/Prostaglandin 20mcg/mL, Papaverine recall — FDA D-0733-2018
Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns may not be sufficient to support the…
Class IIFDA: TerminatedVitalab Pharmacy, Inc.
DrugMay 16, 2018
Vitalab Pharmacy Papaverine 9mg/Phentolamine 1mg/Atropine 0.1mg/Prostaglandinl 10mcg/ml recall — FDA D-0730-2018
Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns may not be sufficient to support the…
Class IIFDA: TerminatedVitalab Pharmacy, Inc.
DrugMay 16, 2018
Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle recall — FDA D-0727-2018
Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugMay 16, 2018
Minivelle recall — FDA D-0863-2018
Defective Delivery System: no longer meets the specification for shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could experience…
Class IIFDA: TerminatedNoven Pharmaceuticals, Inc.
DrugMay 16, 2018
Vitalab Pharmacy Methionine 25mg/Inositol 50mg/Choline 50mg/Cyanocobalamin 1mg/ml, Sterile recall — FDA D-0731-2018
Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns may not be sufficient to support the…
Class IIFDA: TerminatedVitalab Pharmacy, Inc.
DrugMay 16, 2018
Vitalab Pharmacy Papaverine 30mg/Phentolamine 1.5mg/Prostaglandin 50mcg/mL, sterile recall — FDA D-0732-2018
Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns may not be sufficient to support the…
Class IIFDA: TerminatedVitalab Pharmacy, Inc.
DrugMay 16, 2018
Vitalab Pharmacy Methylcobalamin for injection, 1mg/mL and 10 mg/mL, Sterile injectable recall — FDA D-0728-2018
Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns may not be sufficient to support the…
Class IIFDA: TerminatedVitalab Pharmacy, Inc.
DrugMay 16, 2018
Minivelle recall — FDA D-0862-2018
Defective Delivery System: no longer meets the specification for shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could experience…
Class IIFDA: TerminatedNoven Pharmaceuticals, Inc.
DrugMay 16, 2018
Coast Quality Pharmacy Macroaggregated albumin (MAA) kit recall — FDA D-0801-2018
Lack of Assurance of Sterility
Class IIFDA: TerminatedCoast Quality Pharmacy LLC
Medical DeviceMay 9, 2018
Beijing Syntech Laser Trixel C02 Laser surgical lasers recall — FDA Z-1489-2018
The noncompliance is that the certification label was not affixed on the product, with statement "Complies with 21 CFR 1040.10 and 1040.11 except for deviations pursuant to Laser Notice No.…
Class IIFDA: OngoingBeijing Syntech Laser Co., Ltd
Medical DeviceMay 9, 2018
Roche Diagnostics Cobas b 221<4>Roche OMNI S4 system recall — FDA Z-1611-2018
The software responsible for starting scheduled AutoQC measurements (scheduler) will not activate.
Class IIFDA: TerminatedRoche Diagnostics Corporation
Medical DeviceMay 9, 2018
Becton Dickinson & Co BD MAX DNA MMK Lab Use, catalog no. 442828 recall — FDA Z-1545-2018
The package insert incorrectly lists the volume of the primer and probe diluent to use for the reconstitution of the master mix tube. Adding the incorrect amount of diluent could have an…
Class IIIFDA: TerminatedBecton Dickinson & Co.
About the 2018 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.