Class I — King Systems Corp. dba Ambu, Inc.
| Recalling firm | KING SYSTEMS |
|---|---|
| Registered facility | KING SYSTEMS CORPORATION. (the firm's only registered facility) |
| Classification | Class I |
| Status | Terminated |
| Reason | Exhibiting a reversed image. Although the image may appear normal, the users actions will be reversed on the display for left and right directions. |
| Product | King Vision Video Adapter Size 1/2. Laryngoscope used to examine and visualize a patients upper airway and aid in the placement of a tracheal tube. Model Number: KVLVA12 |
| Quantity | 171 units |
| Distribution | Worldwide distribution. US Nationwide, Australia, Belgium, Bolivia, Canada, Costa Rica, Germany, Hong Kong, India, Italy, Japan, Myanmar, Poland, Spain, and UK. |
| Initiated | 2019-11-05 |
| Classified | 2020-02-04 |
| Terminated | 2021-03-23 |
| Recall number | Z-0916-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class I recall — King Systems Corp. dba Ambu, Inc. (Z-0916-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/84415/
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