King Vision Video Adapter Size 1/2 — Class I medical device recall Z-0916-2020
Terminated recall by King Systems Corp. dba Ambu, Inc., reported 2020-02-12, distributed nationwide. Exhibiting a reversed image. Although the image may appear normal, the users actions will be reversed on the d
| Recall number | Z-0916-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | King Systems Corp. dba Ambu, Inc., Noblesville, IN, United States |
| Recall initiated | 2019-11-05 |
| Classified | 2020-02-04 |
| Reported by FDA | 2020-02-12 |
| Terminated | 2021-03-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, BO, CA, CR, DE, ES, GB, HK, IN, IT, JP, PL |
| Quantity | 171 units |
| Lot numbers | 010614, 010629, 010657, 010668, 010670, 010722 |
| Serial numbers | LHXXXXXXX10240, LHXXXXXXX10243, LHXXXXXXX10284, LHXXXXXXX10554, LHXXXXXXX10559, LHXXXXXXX10562, LHXXXXXXX10569, LHXXXXXXX10570, LHXXXXXXX10611, LHXXXXXXX10666 |
| Model numbers | KVLVA12 |
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
Reason for recall
Exhibiting a reversed image. Although the image may appear normal, the users actions will be reversed on the display for left and right directions.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0916-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.