Medical DeviceAug 5, 2020
TELEFLEX MEDICAL Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) recall — FDA Z-2731-2020
Breaking at the point of a welded joint
Class IIFDA: TerminatedTELEFLEX MEDICAL Inc.
Monthly breakdown
2020 recalls by month
Select a month to review the recall records reported during that period.
December 2020315 records · 4 categoriesNovember 2020241 records · 4 categoriesOctober 2020416 records · 4 categoriesSeptember 2020371 records · 4 categoriesAugust 2020245 records · 4 categoriesJuly 2020442 records · 4 categoriesJune 2020342 records · 4 categoriesMay 2020315 records · 4 categoriesApril 2020422 records · 4 categoriesMarch 2020368 records · 4 categoriesFebruary 2020551 records · 4 categoriesJanuary 2020224 records · 4 categories
2020 recalls — page 66
Records are ordered by the best available source date.
Medical DeviceAug 5, 2020
Medtronic Navigation StealthStation" S7 System with Polaris Spectra Camera part number PSU recall — FDA Z-2707-2020
There is a potential for specific camera units to be affected by a characterization issue during manufacturing that results in inaccurate navigation while utilizing both the active and…
Class IIFDA: TerminatedMedtronic Navigation, Inc.
Medical DeviceAug 5, 2020
OrthoPediatrics Orthopedics 6.0MM ROD, COCR, SINGLE HEX, 500MM LENGTH-The RESPONSE" 5.5/6.0 recall — FDA Z-2742-2020
Product may have incorrect laser etched alignment lines, the non-conforming laser etch may have compromised strength, lead to unintended fracture of the device
Class IIFDA: OngoingOrthoPediatrics Corp
Medical DeviceAug 5, 2020
Ion Beam Applications S.A Proteus 235 The Proton Therapy System - Proteus 235 recall — FDA Z-2715-2020
IBA became aware of an issue to resume aborted irradiations because the plan to complete the treatment cannot be loaded.
Class IIFDA: TerminatedIon Beam Applications S.A.
Medical DeviceAug 5, 2020
TELEFLEX MEDICAL Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) recall — FDA Z-2726-2020
Breaking at the point of a welded joint
Class IIFDA: TerminatedTELEFLEX MEDICAL Inc.
FoodAug 5, 2020
Greenhead Lobster Products 1 recall — FDA F-1031-2020
Ready-to-eat lobster meat may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedGreenhead Lobster Products
FoodAug 5, 2020
BUILT BRANDS Peanut Butter Chocolate covered protein bars, packaged in recall — FDA F-1039-2020
Products may be moldy prior to the end of the stated shelf life.
Class IIFDA: TerminatedBUILT BRANDS LLC
FoodAug 5, 2020
Happy Colon Yum Shortbread Cookie 0.98oz UPC 56817 00704 recall — FDA F-1032-2020
Undeclared milk, product contains butter but does not list milk
Class IIFDA: TerminatedHappy Colon Foods
FoodAug 5, 2020
Happy Colon MMMM Chocolate Chip Cookie 0.98oz UPC 56817 00703 recall — FDA F-1033-2020
Undeclared milk, product contains butter but does not list milk
Class IIFDA: TerminatedHappy Colon Foods
FoodAug 5, 2020
BUILT BRANDS S'Mores Chocolate covered protein bars, packaged in metalized recall — FDA F-1040-2020
Products may be moldy prior to the end of the stated shelf life.
Class IIFDA: TerminatedBUILT BRANDS LLC
FoodAug 5, 2020
BUILT BRANDS Toffee Almond Chocolate covered protein bars, packaged in recall — FDA F-1042-2020
Products may be moldy prior to the end of the stated shelf life.
Class IIFDA: TerminatedBUILT BRANDS LLC
FoodAug 5, 2020
BUILT BRANDS Cashew Caramel with Coconut Chocolate covered protein bars recall — FDA F-1036-2020
Products may be moldy prior to the end of the stated shelf life.
Class IIFDA: TerminatedBUILT BRANDS LLC
FoodAug 5, 2020
BUILT BRANDS Cookie Dough Chocolate covered protein bars, packaged in recall — FDA F-1037-2020
Products may be moldy prior to the end of the stated shelf life.
Class IIFDA: TerminatedBUILT BRANDS LLC
FoodAug 5, 2020
BUILT BRANDS Black Cherry Chocolate Creme Chocolate covered protein bars recall — FDA F-1041-2020
Products may be moldy prior to the end of the stated shelf life.
Class IIFDA: TerminatedBUILT BRANDS LLC
FoodAug 5, 2020
BUILT BRANDS Banana Nut Bread Chocolate covered protein bars, packaged in recall — FDA F-1034-2020
Products may be moldy prior to the end of the stated shelf life.
Class IIFDA: TerminatedBUILT BRANDS LLC
FoodAug 5, 2020
Winter Gardens Quality Foods Whole Foods Spinach Artichoke Dip ,4-12 oz containers, Lot # recall — FDA F-1046-2020
The product has been recalled due to undeclared (allergen) egg
Class IFDA: TerminatedWinter Gardens Quality Foods, Inc.
FoodAug 5, 2020
BUILT BRANDS Double Chocolate Mousse Chocolate covered protein bars recall — FDA F-1038-2020
Products may be moldy prior to the end of the stated shelf life.
Class IIFDA: TerminatedBUILT BRANDS LLC
FoodAug 5, 2020
Giant Eagle Net Wt recall — FDA F-1043-2020
Giant Eagle, Inc. has issued a voluntary recall of Giant Eagle Dried Island Fruit Mix,Net Wt. 10 oz., Expiration date 01/15/2021 due to the possibility the product may contain undeclared…
Class IIFDA: TerminatedGiant Eagle
FoodAug 5, 2020
J F C International Kasugai brand Matcha Ame recall — FDA F-1044-2020
Undeclared soybean which is contained in lubricant in candy mold.
Class IIFDA: TerminatedJ F C International Inc.
FoodAug 5, 2020
Stick E Fingers BBQ packaged in 13.2 oz plastic jar, UPC 8 60003 24004 5 recall — FDA F-1047-2020
Ingredients statement declares butter but does not declare milk or buttermilk.
Class IIFDA: TerminatedStick E Fingers BBQ LLC
FoodAug 5, 2020
BUILT BRANDS Banana Chocolate Creme Chocolate covered protein bars recall — FDA F-1035-2020
Products may be moldy prior to the end of the stated shelf life.
Class IIFDA: TerminatedBUILT BRANDS LLC
DrugAug 5, 2020
POLARIZED Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles recall — FDA D-1412-2020
CGMP Deviations: Product was found to be below the label claim for ethanol content and the presence of undeclared methanol.
Class IIFDA: TerminatedPOLARIZED LLC
DrugAug 5, 2020
UVT Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles recall — FDA D-1407-2020
Chemical Contamination: Product contains undeclared methanol.
Class IFDA: TerminatedUVT Inc.
DrugAug 5, 2020
SUN PHARMACEUTICAL INDUSTRIES Clonazepam Orally Disintegrating Tablets, USP, 0.125 mg recall — FDA D-1445-2020
Cross contamination with other products - OOS discovered during routine stability testing for highest unknown impurity later identified as clozapine
Class IIIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
About the 2020 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.