Hernia Pack, Kit number AMS1519 convenience custom kits used for general surgery in hospital operating room
Reported: October 26, 2016 Initiated: April 22, 2015 #Z-0208-2017
Product Description
Hernia Pack, Kit number AMS1519 convenience custom kits used for general surgery in hospital operating room
Reason for Recall
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.
Details
- Recalling Firm
- Windstone Medical Packaging, Inc.
- Units Affected
- 765 kits
- Distribution
- Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.
- Location
- Billings, MT
Frequently Asked Questions
What product was recalled? ▼
Hernia Pack, Kit number AMS1519 convenience custom kits used for general surgery in hospital operating room. Recalled by Windstone Medical Packaging, Inc.. Units affected: 765 kits.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 26, 2016. Severity: Moderate. Recall number: Z-0208-2017.
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