FDA Device recall Z-2636-2024

McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only

FDA Device
Class I
ongoing
Published 2024-08-28

On 2024-08-28 the FDA classified a Class I recall of McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only by Covidien, citing battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2636-2024
Classification	Class I
Status	ongoing
Initiated	2024-07-09
Published	2024-08-28
Last updated	2026-09-13 11:57 UTC
Company	Covidien
Distribution	US

Product

McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only

Reason

Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.

Identifiers

code_info	UDI: 15060272980020 05060272980023 F0602729800201/ All serial Numbers prior to 366170 and Lot/serial number: 370723 370… UDI: 15060272980020 05060272980023 F0602729800201/ All serial Numbers prior to 366170 and Lot/serial number: 370723 370727 370729 370733 370756 370757 370759 370760 370762 370763 370764 370766 370767 370768 370769 370770 370772 370773 370774 370775 370776 370777 370778 370779 370842 370898 370900 370901 370902 370904 370905 370907 370908 370911 370913 370917 370938 370939 370940 370941 370966 370967 370984 370985 370988 370992 371000 371002 371012 371016 371018 371037 371064 371065 371066 371067 371068 371069 371070 371071 371072 371074 371076 371109 371113 371114 371115 371116 371117 371118 371119 371121 371122 371123 371124 371125 371126 371127 371128 371130 371131 371132 371135 371136 371138 371139 371140 371141 371142 371144 371145 371146 371172 371173 371175 371176 371177 371180 371181 371182 371183 371184 371185 371186 371188 371189 371190 371192 371193 371194 371195 371230 371232 371234 371235 371236 371242 371244 371245 371247 371248 371249 371252 371253 371254 371255 371259 37

code_info

UDI: 15060272980020 05060272980023 F0602729800201/ All serial Numbers prior to 366170 and Lot/serial number: 370723 370…

UDI: 15060272980020 05060272980023 F0602729800201/ All serial Numbers prior to 366170 and Lot/serial number: 370723 370727 370729 370733 370756 370757 370759 370760 370762 370763 370764 370766 370767 370768 370769 370770 370772 370773 370774 370775 370776 370777 370778 370779 370842 370898 370900 370901 370902 370904 370905 370907 370908 370911 370913 370917 370938 370939 370940 370941 370966 370967 370984 370985 370988 370992 371000 371002 371012 371016 371018 371037 371064 371065 371066 371067 371068 371069 371070 371071 371072 371074 371076 371109 371113 371114 371115 371116 371117 371118 371119 371121 371122 371123 371124 371125 371126 371127 371128 371130 371131 371132 371135 371136 371138 371139 371140 371141 371142 371144 371145 371146 371172 371173 371175 371176 371177 371180 371181 371182 371183 371184 371185 371186 371188 371189 371190 371192 371193 371194 371195 371230 371232 371234 371235 371236 371242 371244 371245 371247 371248 371249 371252 371253 371254 371255 371259 37

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2636-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.