Medtronic Recall: Best Practices kits containing certain production lots of Clearify Vis
Medtronic Recall: Best Practices kits containing certain production lots of Clearify Vis is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Medtronic; Product: Best Practices kits containing certain production lots of Clearify Visualization System Item Code: 21-345 Intended to be used pri
| Recalling firm | Medtronic |
|---|---|
| Product | Best Practices kits containing certain production lots of Clearify Visualization System Item Code: 21-345 Intended to be used prior to and during endoscopic and laparoscopic procedures to prevent fogging of the scope as well as clean the scope lens |
| Reason for recall | Product sterility is compromised due to breach of the sterile barrier |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide Distribution - US (Nationwide) Foreign: Austria Belgium Bulgaria Brazil Chile Cyprus Denmark Egypt Finland France France Germany Greece Hungary Iran Ireland Israel Italy Japan Kenya Kuwait Latvia Luxembourg Mexico Namibia Netherlands Nigeria Norway Poland Portugal Romania Saudi Arabia Serb |
| Recall initiated | 20161004 |
| Recall number | Z-0890-2017 |
| Category | device |
| State | CT |
| Country | United States |
$29/mo
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