King Systems Issues Recall of King Vision Video Laryngoscope Video Adapter Size 1/2

Company Announcement Date:
January 24, 2020
FDA Publish Date:
January 24, 2020
Product Type:
Medical Devices
Reason for Announcement:
Device exhibits a reversed image
Company Name:
King Systems
Brand Name:
King Vision
Product Description:
Laryngoscope Adapter
Company Announcement
On November 5, 2019, King Systems initiated a voluntary recall of One-Hundred Seventy-One (171) units of its King Vision Video Laryngoscope Adapter Size 1/2. The affected products have been found to exhibit a reversed image, which could potentially result in difficulty navigating during intubation and/or delay in intubation.
The affected product(s) should NOT be used. All affected product(s) should be returned to King Systems.
Affected product was manufactured from April 2nd to September 19th, 2019 and distributed from August 2nd to October 25th, 2019.
The recall includes the following affected devices:
Part Number
Lot Numbers
Serial Numbers
KVLVA12
010614
010629
010657
010668
010670
010722
LHXXXXXXX10240
LHXXXXXXX10243
LHXXXXXXX10284
LHXXXXXXX10554
LHXXXXXXX10559
LHXXXXXXX10562
LHXXXXXXX10569
LHXXXXXXX10570
LHXXXXXXX10611
LHXXXXXXX10666
Affected product can be identified by reviewing the product packaging for Lot Number or individual devices for Serial Number. The Serial Number is located inside the Adapter (Figure 1).
King Systems voluntarily recalled the products after receiving reports of some products exhibiting a reversed image. Although the image may appear normal, the user’s actions will be reversed on the Display for left and right directions. Up and down directions are unaffected (Figure 2). As of January 20th, 2020, King Systems has not received any reports of adverse events (no patient injuries) resulting from this issue. FDA has been notified of this action.
King Systems has notified impacted distributors and customers and is arranging for return and credit/replacement of all recalled product(s).
A total of One-Hundred and Seven (107) affected products were shipped to distributors and customers in the USA (AK, AL, CA, FL, IA, IL, KS, LA, MD, MN, MS, NC, NE, PA, SC, TX, WA, and WI) and Sixty-Four (64) were shipped internationally (Argentina, Australia, Belgium, Bolivia, Canada, Costa Rica, Germany, Hong Kong, India, Italy, Japan, Myanmar, Poland, Spain, and UK).
Consumers with questions may contact the company by phone at +1 (410) 768-6464 between the hours of 8:00am and 5:00pm EST or by emailing Shelby Mitchell at shmi@ambu.com .
Adverse reactions or quality problems experienced with the use of this product may be reported to FDA:
Complete and submit the report Online
Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

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