FDAClass IIOctober 26, 2016

Newport Coast Basic Pack recall: Sterility Concern

Newport Coast Basic Pack, Kit number 007484-1 convenience custom kits used for general surgery in hospital operating room

Why was Newport Coast Basic Pack recalled?

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the custom AMS kit were recalled because gloves may contain splits or holes compromising sterility.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot Numbers/ Expiration Dates: 59310 7/9/2015 63339 11/11/2015 61486 11/27/2015 65400 11/30/2015 65399 12/26/2015 67044 4/5/2016 67905 5/13/2016 75637 6/25/2016 74959 8/5/2016 71107 8/11/2016 71635 8/29/2016 74764 1/15/2017 78706 9/26/2017

Product
Newport Coast Basic Pack, Kit number 007484-1 convenience custom kits used for general surgery in hospital operating room
Recalling firm
Windstone Medical Packaging, Inc.
Quantity
280 kits
Distribution
Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.
Recall date
October 26, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls