CLASS I Device recall · Reported 12 Feb 2020 · FDA Enforcement Report
King Vision Video Adapter Size 1/2 recalled by King Systems
King Systems is recalling King Vision Video Adapter Size 1/2, distributed nationwide in the US. The recall was initiated on 5 Nov 2019 and the FDA has classified it as Class I.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0916-2020
- FDA event ID
- 84415
- Recalling firm
- King Systems, Noblesville, IN
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 5 Nov 2019
- FDA classified
- 4 Feb 2020
- Reported
- 12 Feb 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Device type
- Masks, Gloves & PPE
Timeline
| 5 Nov 2019 | Recall initiated by company | |
| 4 Feb 2020 | Classified by FDA | +91 days |
| 12 Feb 2020 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Product as listed by the FDA
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
Where it was distributed
Worldwide distribution. US Nationwide, Australia, Belgium, Bolivia, Canada, Costa Rica, Germany, Hong Kong, India, Italy, Japan, Myanmar, Poland, Spain, and UK.
Questions about this recall
Is King Vision Video Adapter Size 1/2 recalled?
Yes. King Systems recalled King Vision Video Adapter Size 1/2 on 5 Nov 2019. The recall is Class I and its status is Terminated. Recall number Z-0916-2020.
Why was it recalled?
Exhibiting a reversed image. Although the image may appear normal, the users actions will be reversed on the display for left and right directions.
Which lots are affected?
Lot codes: 010614, 010629, 010657, 010668, 010670, 010722; Serial Numbers: LHXXXXXXX10240 LHXXXXXXX10243 LHXXXXXXX10284 LHXXXXXXX10554 LHXXXXXXX10559 LHXXXXXXX10562 LHXXXXXXX10569 LHXXXXXXX10570 LHXXXXXXX10611 LHXXXXXXX10666
Where was it sold?
Worldwide distribution. US Nationwide, Australia, Belgium, Bolivia, Canada, Costa Rica, Germany, Hong Kong, India, Italy, Japan, Myanmar, Poland, Spain, and UK.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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