Windstone Medical Packaging, Inc. recalls Laparotomy Pack Latex Free, part number 007725-7. This is a custom convenience surgical instrument disposable kit. Ther…
- Recall date
- March 21, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1869-2016
- FDA classification
- Class II
- Brand / firm
- Windstone Medical Packaging, Inc.
- Sold / distributed
- Nationwide distribution to Louisiana and Montana.
Why it was recalled
These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges which were recalled by Medtronic due to the potential for sterile barrier to be comprised at the packaging seal.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Laparotomy Pack Latex Free, part number 007725-7. This is a custom convenience surgical instrument disposable kit. There are multiple component in this kit and the recalled item subject to recall is Medtronic Kerlix X-Ray Detectable Laparotomy Sponges.
Get recall alerts
Free email alert whenever Windstone Medical Packaging, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Windstone Medical Packaging, Inc.