FDA recall record

Karl Storz SE & Co recall — FDA Z-1618-2020

The firm has become aware that there is a potential that the glass cover at the distal end of the camera/led lighting on the video laryngoscope could…

Class IIclassification
Z-1618-2020official record ID
Apr 8, 2020report date

Recall record at a glance

Official recordZ-1618-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKarl Storz Endoscopy
Report dateApr 8, 2020
Recall initiation dateDec 6, 2019
Quantity27,165 scopes
LocationEl Segundo, CA, United States

Official product description

Karl Storz SE & Co. KG, C-MAC Video Laryngoscope MIL # 1, for the following REF numbers: 1. 8403xx series, which includes: 8403AX, AXC, BX, BXC, DXC, EXC, GXC, HX, HXK, HXP, KXC, MXC 2. 8401xx series, which includes: 8401AX, AXC, BX, BXC, DXC, GXC, HX, HXP, KXC. Product Usage: Video Laryngoscopes are used to visualize the airways and vocal cords during endotracheal intubation and for the inspection and examination of the upper respiratory tract. Video Laryngoscopes are designed for transient use in invasive procedures through a body orifice.

Why the product was recalled

The firm has become aware that there is a potential that the glass cover at the distal end of the camera/led lighting on the video laryngoscope could become loose during reprocessing or use. If this occurs during usage, it may result in a delay in procedure and/or require removal from body.

Distribution information

Worldwide distribution - US Nationwide and country of Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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