Dornier Medtech America, Inc. Recall: Dornier Diode Laser Fibers:Used with Dornier Medilas
Dornier Medtech America, Inc. Recall: Dornier Diode Laser Fibers:Used with Dornier Medilas is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Dornier Medtech America, Inc.; Product: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers Part Number/Description: K1001291 600
| Recalling firm | Dornier Medtech America, Inc. |
|---|---|
| Product | Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers Part Number/Description: K1001291 600 micron single use fiber K2011824 600 micron single use fiber K1001293 600 micron single use fiber K2011826 600 micron 5X reusable fiber K1008084 600 micron single use fiber K2011828 400 micron 5X reusable fiber K1010500 600 micron fibertome fiber K2012021 600 micron single use fiber K1015640 AngioSpot Fiber Kit K2012393 600 micron single use fiber K2010292 400 micron single use fiber K2012439 600 micron 5X reusable fiber K2010667 micron ITT fiber K2012875 600 micron 3X reusable fiber K201 |
| Reason for recall | Pin hole package failures compromising sterility of product |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US Nationwide distribution. |
| Recall initiated | 20190401 |
| Recall number | Z-1381-2019 |
| Category | device |
| State | GA |
| Country | United States |
$29/mo
Try RecallGuard →