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

For Immediate Release	King Systems
	15011 Herriman Blvd.
	Noblesville Indiana, 46060
	[phone]
	20 January 2020

King Systems Issues Recall of King

Vision Video Laryngoscope Video

Adapter Size 1/2

Noblesville, IN - On November 5, 2019, King Systems initiated a voluntary recall of One-HundredSeventy-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	LHXXXXXXX10240
	010629	LHXXXXXXX10243
	010657	LHXXXXXXX10284
	010668	LHXXXXXXX10554
	010670	LHXXXXXXX10559
	010722	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, 15011 Herriman Blvd., Noblesville Indiana, 46060

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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 (Fig- ure 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 [phone] between the hours of 8:00am and 5:00pm EST or by emailing Shelby Mitchell at [e-mail].

Adverse reactions or quality problems experienced with the use of this product may be reported to FDA:

• Online athttp://www.fda.gov/Safety/MedWatch/HowToReport/default.htm
• Call FDA1-800-FDA-1088

Figure 1: KVLVA12 Serial Number location.

Figure 2: KVLVA12 exhibiting a reversed image.

King Systems, 15011 Herriman Blvd., Noblesville Indiana, 46060

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