FDA Device recall Z-2637-2024
McGRATH" MAC EMS Video Laryngoscope, REF: 300-200-000 , 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 EMS Video Laryngoscope, REF: 300-200-000 , 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-2637-2024 |
| 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 EMS Video Laryngoscope, REF: 300-200-000 , 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: 15060272980112. All serial Numbers prior to 366170 and Lot/Serial Numbers:373090 366392 366474 372653 372729 37297…UDI: 15060272980112. All serial Numbers prior to 366170 and Lot/Serial Numbers:373090 366392 366474 372653 372729 372974 373035 373044 373063 373086 373504 373507 377641 377646 377653 377667 377669 377924 378165 378301 378318 378417 378420 378471 382906 383017 383303 383304 383386 383394 383414 383440 383441 383484 383505 383506 383507 383541 383675 383763 383765 390634 390640 390662 390671 390682 390696 390753 390766 395275 395358 395364 395373 395411 395419 395527 395577 395591 395658 395665 395668 395671 395691 395704 395749 395827 395849 395871 395894 395895 395909 395926 396011 396031 396073 396247 396263 401797 401798 401842 401855 401860 401956 401964 402000 402017 402046 402140 402235 402241 402269 402272 373100 373101 373102 373103 373104 373105 373106 373107 373108 373111 373112 373113 373114 373115 373116 373117 373118 373119 373120 373121 373122 373123 373124 373125 373126 373127 373128 373131 373132 373133 373134 373135 373136 373137 373138 373139 373140 373141 373142 3731 |
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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-2637-2024%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.