Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS MIS Poly Screw Driver B recall — FDA Z-2881-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Latest records
Latest recalls — page 1584
The newest recall records with useful source details are listed here.
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS MISS/MIS Compressor and Rod Tightener recall — FDA Z-2998-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS C recall — FDA Z-3010-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS Poly Screw 6.5 x 35mm recall — FDA Z-2935-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS Poly Screw 6.5 x 55mm recall — FDA Z-2903-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS MIS Pedicle Cut recall — FDA Z-2981-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
International Medsurg Connection Piston Syringe and Hypodermic Needle, 5 CC L/L 22 G X 1.0 recall — FDA Z-2842-2017
Insufficient documentation to support product sterility claims.
Class IIFDA: TerminatedInternational Medsurg Connection, Inc.
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS Distractor recall — FDA Z-2971-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS MIS Screw 7.5 x 40mm recall — FDA Z-2919-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS Guide Wire recall — FDA Z-3015-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS 50mm Curved and precontoured Rod recall — FDA Z-2943-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS 5.5 x 35mm Curved Rod recall — FDA Z-2880-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
International Medsurg Connection Syringe Bulb, 60 CC 50 pcs per case recall — FDA Z-2804-2017
Insufficient documentation to support product sterility claims.
Class IIFDA: TerminatedInternational Medsurg Connection, Inc.
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS MIS Screw 6.5 x 40mm and 6.5 x 4.0 mm screw recall — FDA Z-2927-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
International Medsurg Connection Piston Syringe, 10 CC L/S, 100 per box, 12 boxes/case recall — FDA Z-2856-2017
Insufficient documentation to support product sterility claims.
Class IIFDA: TerminatedInternational Medsurg Connection, Inc.
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS 60mm MIS Rod recall — FDA Z-2895-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS 40mm Rod recall — FDA Z-2957-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS Body Alignment Driver recall — FDA Z-3011-201
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS MIS Screw5.5 x 55mm recall — FDA Z-2925-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
Medical DeviceAug 16, 2017
Valorem Surgical PALLAS M/MAXIMIS 350 Straight Rod recall — FDA Z-2958-2017
Devices are not consistent with Quality System Requirements.
Class IIFDA: TerminatedValorem Surgical LLC
FoodAug 16, 2017
Coborn's Fudge Brownie, Net Wt recall — FDA F-3351-2017
Some Gluten Free Chocolate Chip Bars were incorrectly labeled as Gluten Free Fudge Brownies. The Gluten Free Chocolate Chip Bars that are incorrectly labeled as Gluten Free Fudge Brownies…
Class IIFDA: TerminatedCoborn's, Inc.
FoodAug 16, 2017
Publix Supermarkets NET WT 16 oz recall — FDA F-3360-2017
The reason for recall was that some jars of Publix GreenWise Cashew Butter may actually contain Almond Butter.
Class IIFDA: TerminatedPublix Supermarkets, Inc. (Deli Kitchen)
FoodAug 16, 2017
MCCAIN ONION RING BATTERED PORTION PERFECT ¿ 60X4 oz recall — FDA F-3353-2017
McCain Foods Canada, Inc. initiated a voluntary recall of their frozen MCCAIN ONION RING BATTERED PORTION PERFECT ¿ 60X4 oz following a supplier's recall of a raw ingredient due to…
Class IIFDA: TerminatedMcCain Foods Canada, Inc.
FoodAug 16, 2017
Sunneen Health Foods Whole Foods Market PB & J Parfait Made With Greek Yogurt recall — FDA F-3350-2017
Sunneel Health Foods received a call from their customer indicating some of their Vegan Match Cocoa Parfaits were misbranded as PB & J Parfaits. The ingredient statement failed to declare…
Class IFDA: TerminatedSunneen Health Foods, LLC
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