Lap Band Pack recall: Sterility Concern
Lap Band Pack, Kit number AMS1785(A convenience custom kits used for general surgery in hospital operating room
Why was Lap Band 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: 58289 10/17/2014 60644 2/19/2015 65363 2/28/2015 61474 7/23/2015 65877 11/1/2015 64537 11/30/2015 66998 1/31/2016 68952 1/31/2016 67661 2/29/2016 71625 2/29/2016 70410 4/30/2016 71947 5/31/2016 72877 5/31/2016 57137 6/7/2016 77238 6/30/2016 78143 6/30/2016 73985 8/31/2016 74752 8/31/2016 74973 8/31/2016 76523 8/31/2016
- Product
- Lap Band Pack, Kit number AMS1785(A convenience custom kits used for general surgery in hospital operating room
- Recalling firm
- Windstone Medical Packaging, Inc.
- Quantity
- 390 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)