Allergen Hub
Egg Recalls in the United States
1865 food recalls involving egg tracked from FDA open data. Updated daily.
1865 Egg Recalls
All food recalls →Blueroot Health, Inc. recalls Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, is
Contains undeclared egg, soy, and hazelnut
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F&S Fresh Foods, Inc. recalls ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, peri
Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.
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Orthalign, Inc recalls Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
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Orthalign, Inc recalls Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
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Perfect Pasta, Incorporated recalls Lobster & Crab Ravioli. Keep Frozen. Contains: Wheat, Eggs,
Undeclared shrimp, crab, lobster, pollock (fish), whiting (fish), and soy.
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Ambrosia Brands LLC recalls Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 cap
Product may be contaminated with Salmonella
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Willamette Valley Pie Company, LLC recalls Frozen Raw Bulk 8 inch Blueberry Crumble Pie (4 pies/case).
Potential contamination with listeria monocytogenes.
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House Of Flavors, Inc. recalls House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice
Undeclared egg
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Ajinomoto Foods North America Inc. recalls Item 81153 Kroger Chinese Inspiration Vegetable Fried Rice -
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
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TG FOODS INC recalls Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Po
The product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species of FISH parenthetically or via a Contains statement.
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Exactech, Inc. recalls Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 16o, RI
The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags that did not contain an additional oxygen barrier layer consisting of Ethylene Vinyl Alcohol (EVOH).
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Exactech, Inc. recalls Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 16o, LE
The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags that did not contain an additional oxygen barrier layer consisting of Ethylene Vinyl Alcohol (EVOH).
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Exactech, Inc. recalls Exactech Equinoxe GLENOID, POSTERIOR AUGMENT,PEGGED, CEMENTE
The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags that did not contain an additional oxygen barrier layer consisting of Ethylene Vinyl Alcohol (EVOH).
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Exactech, Inc. recalls Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 12o, LE
The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags that did not contain an additional oxygen barrier layer consisting of Ethylene Vinyl Alcohol (EVOH).
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Exactech, Inc. recalls Exactech Equinoxe GLENOID, POSTERIOR AUGMENT,PEGGED, CEMENTE
The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags that did not contain an additional oxygen barrier layer consisting of Ethylene Vinyl Alcohol (EVOH).
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Exactech, Inc. recalls Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 12o, RI
The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags that did not contain an additional oxygen barrier layer consisting of Ethylene Vinyl Alcohol (EVOH).
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Cardinal Health 200, LLC recalls Convertors Robotic Drape with Attached Leggings; Product is
Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.
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GE Medical Systems Information Technologies, Inc. recalls CARESCAPE Patient Data Module (PDM) v2.6 software used with
Device does not produce a visual or audible impedance respiration APN alarm when an impedance respiration apnea event occurs.
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ZOLL Medical Corporation recalls OneStep CPR Complete, Adult Multi Function Electrodes, Part
A portion of one lot of ZOLL OneStep Complete Electrodes for adults will cause the defibrillator to deliver pediatric energy levels instead of adult energy levels when used with the ZOLL R Series Defibrillator. Defective electrodes will display PEDIATRIC PADS IN USE on the R Series defibrillator. Using the affected product with the M Series Defibrillator poses no risk.
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Encore Medical, Lp recalls Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL,
It was discovered during a surgery that the design of the radius at the base of the pegs of the Anatomic Glenoid Trial (Part Numbers: 804-07-380, 804-07-420, 804-07-460, 804-07-500, and 804-07-540) is much larger on the trails than on the implants
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