FoodOct 30, 2019
Samurai Brand Furikake Popcorn Net Wt recall — FDA F-0086-2020
Undeclared allergen; fish
Class IFDA: TerminatedSamurai, Inc.
October 2019 recalls — page 3
These records include useful source details for the selected month.
FoodOct 30, 2019
Lipari Foods Operating Company, LLC Premo and Fresh Grab Ham & Cheese wheat sandwich, 5 oz. recall — FDA F-0090-2020
Products contain chicken which has been recalled by supplier because it may be contaminated with Listeria monocytogenes
Class IFDA: TerminatedLipari Foods Operating Company, LLC.
FoodOct 30, 2019
Hall Global OXZGEN Performance 25 mg Hemp Derived CBD + Teacrine + BCAA recall — FDA F-0070-2020
Yellow #6 is not declared on ingredient label. Label claim for B2 is incorrect (contains 5 mg not 10 mg as stated).
Class IIFDA: TerminatedHall Global, LLC
FoodOct 30, 2019
Hall Global Sugar Mill Farms Focused Energy 25 mg Hemp Extract Berry recall — FDA F-0071-2020
Yellow #6 is not declared on ingredient label. The label lists Green Coffee Beans as an ingredient, but Guarana Seeds were used instead. The label lists the flavor as berry boost , but…
Class IIFDA: TerminatedHall Global, LLC
FoodOct 30, 2019
Euphoria Fancy Food Capitan K Salmon slightly salted piece - net.wt 1.05 oz recall — FDA F-0072-2020
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedEuphoria Fancy Food Inc.
FoodOct 30, 2019
Roland Brand Black Caviar - Whole Grain Lumpfish recall — FDA F-0057-2020
Potential to be contaminated with Clostridium botulinum.
Class IFDA: TerminatedRoland Foods, LLC
FoodOct 30, 2019
Dole Crushed Pineapple in 100% pineapple juice Manufactured recall — FDA F-0062-2020
Foreign object; potential plastic pieces.
Class IIFDA: TerminatedDole Packaged Foods, LLC
FoodOct 30, 2019
Whole Foods Market Consider Bardwell Farm Dorset cheese PLU code 97776 sliced and recall — FDA F-0129-2020
Potential to contain Listeria monocytogenes
Class IFDA: TerminatedWhole Foods Market
FoodOct 30, 2019
The Newark Nut Store Koppers Chocolate Dark Chocolate Gummy Bears, 4oz recall — FDA F-0074-2020
Kopper s Chocolate has initiated recall of Koppers Chocolate Dark Chocolate Gummy Bears, 4oz (113g) retail package, metallized foil resealable pouch, 12 pouches per case, printed BB:…
Class IIFDA: TerminatedThe Newark Nut Store
FoodOct 30, 2019
Wismettac Asian Foods Shirakiku Buckwheat Noodles Yamaimo Soba With Concentration recall — FDA F-0059-2020
Product label identifies bonito, but product dipping sauce actually contains skipjack tuna, yellowfin tuna, and bluefin tuna as well as does not state the general allergen name of fish.
Class IIFDA: TerminatedWismettac Asian Foods, Inc.
FoodOct 30, 2019
Threshold Enterprises Source Naturals Dietary Supplement Brain Charge Advanced recall — FDA F-0061-2020
Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation.
Class IIIFDA: TerminatedThreshold Enterprises Ltd
FoodOct 30, 2019
The Truck Farm Tia Rita's Spicy Southwestern Green Chile Cornbread dry mix recall — FDA F-0054-2020
The product contains wheat flour, but does not declare wheat on the label.
Class IIFDA: TerminatedThe Truck Farm, LLC
DrugOct 30, 2019
Nephron Pharmaceuticals Corporation dba Nephron PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine recall — FDA D-0149-2020
GMP Deviations: potential glass contamination
Class IIFDA: TerminatedNephron Pharmaceuticals Corporation dba Nephron…
DrugOct 30, 2019
Nephron Pharmaceuticals Corporation dba Nephron PF-Fentanyl Citrate (2 mcg/mL)* & recall — FDA D-0147-2020
GMP Deviations: potential glass contamination
Class IIFDA: TerminatedNephron Pharmaceuticals Corporation dba Nephron…
DrugOct 30, 2019
Nephron Pharmaceuticals Corporation dba Nephron PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine recall — FDA D-0148-2020
GMP Deviations: potential glass contamination
Class IIFDA: TerminatedNephron Pharmaceuticals Corporation dba Nephron…
DrugOct 30, 2019
Nephron Pharmaceuticals Corporation dba Nephron Amino Acid Injection 50 g/1000 mL (50 mg/mL) recall — FDA D-0150-2020
Lack of Assurance of Sterility; bags have potential to leak
Class IIFDA: TerminatedNephron Pharmaceuticals Corporation dba Nephron…
VehicleOct 28, 2019
CX-9 tread/belt recall — NHTSA campaign 19V770000
Mazda North American Operations (Mazda) is recalling certain 2019 CX-9 vehicles equipped with Sumitomo Falken ZIEX CT50 A/S tires, size P255/50R20 104V, having date code 1619. An incorrect…
tread/beltMazda North American Operations
VehicleOct 24, 2019
Chrysler gas recirculation valve (egr valve) recall — NHTSA campaign 19V757000
Chrysler (FCA US LLC) is recalling certain 2014-2019 Ram 1500 and 1500 Classic Pickup trucks equipped with 3.0L Eco Diesel engines. The Exhaust Gas Recirculation (EGR) cooler may crack and…
gas recirculation valve (egr valve)Chrysler (FCA US LLC)
VehicleOct 24, 2019
General Motors wheel speed sensor/tone ring recall — NHTSA campaign 19V761000
General Motors LLC (GM) is recalling certain 2015-2020 Chevrolet Suburban, Tahoe, and GMC Yukon, and 2014-2018 Chevrolet Silverado 1500 and GMC Sierra 1500 vehicles equipped with a…
wheel speed sensor/tone ringGeneral Motors LLC
Medical DeviceOct 23, 2019
Vital Scientific N.V Viva-E, Catalog # 6002-380, UDI # 03661540600050 Product Usage recall — FDA Z-0155-2020
The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.
Class IIFDA: TerminatedVital Scientific N.V.
Medical DeviceOct 23, 2019
ICU Medical Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets recall — FDA Z-0137-2020
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Class IIFDA: TerminatedICU Medical Inc.
Medical DeviceOct 23, 2019
ICU Medical Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets recall — FDA Z-0129-2020
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Class IIFDA: TerminatedICU Medical Inc.
Medical DeviceOct 23, 2019
Siemens Atellica CH 930 Analyzer recall — FDA Z-0148-2020
Atellica CH 930 Analyzer - Erroneous Indices for Hemolysis and Lipemia in Software versions 1.19.2 and below
Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.
Medical DeviceOct 23, 2019
Vital Scientific N.V Selectra ProM Analyzer, Catalog # 6003-435/UDI # 03661540600395 and recall — FDA Z-0157-2020
The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.
Class IIFDA: TerminatedVital Scientific N.V.
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.