Custom Pack - with Introducer Kit recall: Sterility Concern
Custom Pack - with Introducer Kit, Kit number TVS4011NI(K and TVS4011NI(L convenience custom kits used for general surgery in hospital operating room
Why was Custom Pack - with Introducer Kit 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: 62733 11/3/2015 62734 11/11/2015 63822 11/15/2015 63851 1/1/2016 64256 1/3/2016 64255 1/13/2016 63852 4/2/2016 69318 7/14/2016 69233 7/18/2016 69910 9/17/2016 70959 12/6/2016 70958 1/3/2017 73965 1/9/2017 73697 1/20/2017 73698 1/23/2017 75426 5/18/2017 73966 5/20/2017 76637 6/11/2017 76070 6/30/2017 78670 8/13/2017 78276 9/30/2017
- Product
- Custom Pack - with Introducer Kit, Kit number TVS4011NI(K and TVS4011NI(L convenience custom kits used for general surgery in hospital operating room
- Recalling firm
- Windstone Medical Packaging, Inc.
- Quantity
- 1470 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)