McGRATH MAC 301-000-000 (UDI 10884521823396)Recalls & reported problems
Covidien LP · Video Laryngoscope · Class 1
All models of McGRATH MAC (11)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
Quick summary
This McGrath MAC video laryngoscope has 204 adverse event reports, with 6 injuries and no deaths. Most describe a blank screen or failure to power up, and one injury report describes a blade that came off during intubation and stayed in the patient's throat. It has 2 open recalls, one on battery instructions and one on units that failed quality tests and were stolen and sold. Reports fell to 13 in the last 12 months from 187 the year before.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 202
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 2
Summary
The FDA's MAUDE database contains 202 adverse event reports that list this exact device (DI 10884521823396), received between May 8, 2023 and May 5, 2026 — classified as 6 injuries, 196 malfunctions.
The most frequently reported specific device problem is “No Display/Image” (189 reports).
2 FDA recall records name this device's identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Recalls naming this device
- Jul 9, 2024Open, Classified
IFU update to address device's battery handling information.
Z-2717-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 28, 2023Open, Classified
Defective video laryngoscopes that did not pass quality tests established for the product, that were designated for destruction, were stolen, and subsequently distributed for sale. Defective device use may result in failed laryngoscopy and/or intubation.
Z-0144-2024 · Root cause: Process control · Recall details · FDA record ↗
Most reported problems
Device problems
- No Display/Image189
- Electrical /Electronic Property Problem12
- Failure to Power Up10
- Erratic or Intermittent Display7
- Failure to Run on Battery6
- Mechanical Problem6
- Manufacturing, Packaging or Shipping Problem4
- Fitting Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions170
- Insufficient Information29
- Unspecified Tissue Injury3
- Foreign Body In Patient2
- Bradycardia1
- Cardiac Arrest1
- Device Embedded In Tissue or Plaque1
- Respiratory Failure1
Recent adverse event reports
The 25 most recent of 202 reports, in the reporter's own words as published by the FDA.
InjuryMay 5, 2026Fitting Problem
IT WAS REPORTED THAT THE VIDEOLARYNGOSCOPE WITH SIZE 3 BLADE WAS USED AND THE PATIENT WAS SUCCESSFULLY INTUBATED IN THE FIELD . WHEN THE HOSPITAL EXTUBATED THE PATIENT AFTER 5 DAYS IT WAS DISCOVERED THAT THE BLADE WAS STILL IN THE PATIENT'S THROAT. IT SEEMS THAT THE BLADE DID NOT LATCH ONTO THE HANDLE AS EXPECTED AND CAME OFF THE HANDLE DURING INTUBATION. IT WAS MADE SURE THAT THE BLADE WAS STILL INTACT AND NOT MISSING ANY PIECES WHEN REMOVED. THE PATIENT WAS ALIVE BUT AN IDENTIFIED INJURY WAS REPORTED.
Patient problems: Device Embedded In Tissue or Plaque; Foreign Body In Patient; Unspecified Tissue Injury
MAUDE report 25088451 ↗InjuryMay 5, 2026Fitting Problem
IT WAS REPORTED THAT THE PATIENT WAS SUCCESSFULLY INTUBATED AND WHEN THE CREW WENT TO APPLY THE TUBE TAMER, IT WAS NOTICED THAT THE SIZE 3 BLADE HAD COME OFF THE HANDLE AND WAS STILL IN THE PATIENT'S THROAT. THE CREW REMOVED THE BLADE AND THEN APPLIED THE TUBE TAMER. A COUPLE OF DIFFERENT BLADES WAS TESTED TO THE HANDLE, AND IT LOOKS LIKE THE SIZE 3 BLADE WOULD NOT LATCH ONTO THE HANDLE CORRECTLY. THE OTHER SIZE BLADES LATCH ONTO THE HANDLE FINE. THE PATIENT WAS ALIVE BUT AN IDENTIFIED INJURY WAS REPORTED.
Patient problems: Foreign Body In Patient; Unspecified Tissue Injury
MAUDE report 25088445 ↗MalfunctionApr 30, 2026No Display/Image; Failure to Power Up
IT WAS REPORTED THAT A HEALTHCARE PROFESSIONAL USED THE VIDEO LARYNGOSCOPE DURING A DIFFICULT INTUBATION AND, WHEN THE HANDLE WAS TU RNED ON, A BLUE SCREEN DISPLAYED AND IT DID NOT PROGRESS TO THE VIDEO SCREEN. AFTER THE BATTERY WAS CHANGED, THE VIDEO SCREEN APPEARED BUT THEN WENT BLACK DURING THE INTUBATION. IT WAS FURTHER REPORTED THAT THE HANDLE WOULD NOT TURN ON. THE HANDLE WAS TESTED WITH KNOWN GOOD BATTERIES, BUT THE ISSUE WAS NOT RESOLVED. THE ANESTHETIST WAS ABLE TO INTUBATE WITHOUT IT IN THE END AS THE SCREEN WAS NOT RELIABLE. THERE WAS NO PATIENT INJURY.
Patient problems: Insufficient Information
MAUDE report 25043599 ↗MalfunctionApr 28, 2026No Display/Image
IT WAS REPORTED THAT THE LIGHT-EMITTING DIODE (LED) OF THE VIDEOLARYNGOSCOPE WAS ON BUT HAD NO DISPLAY EVEN THE BATTERY ICON WAS NOT DISPLAYED PRIOR TO USE. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25017250 ↗MalfunctionApr 24, 2026No Display/Image
IT WAS REPORTED THAT THE VIDEO LARYNGOSCOPE'S SCREEN DID NOT WORKED AND HAD A BLACK SCREEN. IT WAS UNKNOWN IF THERE WAS PATIENT INVOLVEMENT AT THE TIME OF THE REPORTED EVENT.
Patient problems: Insufficient Information
MAUDE report 24987758 ↗MalfunctionApr 22, 2026No Display/Image
IT WAS REPORTED THAT THE VIDEOLARYNGOSCOPE TURNS ON, BUT THERE WAS NO DISPLAY AND THE DEVICE DID NOT FUNCTION PROPERLY. THE BATTERY WAS REPLACED, BUT THE ISSUE DID NOT IMPROVED PRIOR TO USE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24954109 ↗MalfunctionApr 6, 2026No Display/Image
IT WAS REPORTED THAT, WHILE PREPARING FOR USE, THE CUSTOMER ATTEMPTED TO POWER ON THE VIDEOLARYNGOSCOPE AND THE SCREEN STARTED UP BUT THEN WENT BLACK. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24794623 ↗MalfunctionMar 17, 2026No Display/Image
IT WAS REPORTED THAT PRIOR TO USE, THE VIDEOLARYNGOSCOPE SCREEN DID NOT DISPLAY EVEN THOUGH IT WAS REPLACED WITH A NEW BATTERY. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24624313 ↗MalfunctionMar 5, 2026No Display/Image
IT WAS REPORTED THAT THE VIDEOLARYNGOSCOPE HAD THE LIGHT-EMITTING DIODE (LED) ON BUT THE SCREEN DID NOT CAME OUT. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24518118 ↗MalfunctionJan 16, 2026No Display/Image
IT WAS REPORTED THAT THE LIGHT OF THE VIDEOLARYNGOSCOPE COME ON BUT THE SCREEN STILL BLACK PRIOR TO USE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24093072 ↗MalfunctionNov 26, 2025No Display/Image; Failure to Shut Off; No Display/Image; Failure to Shut Off
IT WAS REPORTED THAT THE VIDEOLARYNGOSCOPE DID NOT DISPLAY A VIDEO IMAGE DESPITE SEVERAL BATTERIES BEING TRIED AND THE SCOPE LIGHT REMAINED ON UNTIL THE BATTERY WAS REMOVED. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23662845 ↗MalfunctionOct 20, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT DURING TESTING/MAINTENANCE, THE VIDEO LARYNGOSCOPE HAD NO IMAGE ON DISPLAY. EVEN AFTER TURNING THE POWER ON AND OFF REPEATEDLY. TRIED VARIOUS BATTERIES WITH SAME OUTCOME. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23337052 ↗MalfunctionSep 19, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT DURING TESTING/MAINTENANCE, THE VIDEO LARYNGOSCOPE'S DISPLAY DID NOT COME ON EVEN THOUGH THE UNIT LIGHTS UP. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23100693 ↗MalfunctionSep 18, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT THE HANDLE HAD NO DISPLAY BEFORE USE. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23089610 ↗MalfunctionSep 12, 2025No Display/Image; Electrical /Electronic Property Problem; No Display/Image; Electrical /Electronic Property Problem
IT WAS REPORTED THAT DURING TESTING, THE VIDEOLARYNGOSCOPE EXHIBITED A BLANK DISPLAY AND HAD A BLUE SCREEN. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23038819 ↗MalfunctionSep 10, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT THE DEVICE HAD NO IMAGE ON THE DISPLAY EVEN AFTER THE BATTERY BEING SWAPPED, THOUGH THE BLADE DID LIGHT UP. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23019198 ↗MalfunctionSep 10, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT DURING TESTING, THE VIDEOLARYNGOSCOPE'S SCREEN WAS NOT WORKING, WITH THE LIGHT ON THE END OF THE SCOPE TURNING ON BUT THE SCREEN ONLY FLASHING BLUE AND THEN RETURNING TO BLACK. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23019155 ↗MalfunctionSep 9, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT PRIOR TO USE, THE SCREEN OF THE VIDEOLARYNGOSCOPE HAD NO DISPLAY. THE BATTERY WAS REPLACED BUT THE SITUATION DID NOT IMPROVED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23000495 ↗MalfunctionAug 19, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT THE DISPLAY SCREEN OF THE VIDEOLARYNGOSCOPE WAS BLACK WITH NO IMAGE DURING PRE-OPERATIVE PREPARATION. ALL TROUB LESHOOTING STEPS WERE PERFORMED AND THE BATTERY WAS REPLACED, BUT THE DISPLAY ISSUE PERSISTED. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22846428 ↗MalfunctionJul 30, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT UPON TURNING ON THE HANDLE, THE DEVICE SCREEN TURNED COMPLETELY BLANK MOST OF THE TIME DURING USE. SEVERAL DIFFERENT BATTERIES WERE USED IN AN ATTEMPT TO TROUBLESHOOT THE ISSUE, BUT THESE EFFORTS WERE UNSUCCESSFUL. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22668842 ↗MalfunctionJul 28, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT PRIOR TO USAGE, THE VIDEO LARYNGOSCOPE'S SCREEN HAD NO DISPLAY. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22639284 ↗MalfunctionJul 23, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT THE VIDEOLARYNGOSCOPE'S LED LIGHT ON THE DISPLAY WOULD LIGHT UP, BUT THERE WAS NO BATTERY ICON DISPLAYED EVEN AFTER REPLACING THE BATTERY. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22579900 ↗MalfunctionJul 14, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT THE DEVICE SHOWED A BLANK SCREEN AFTER IT POWERED ON DURING TESTING. THE CUSTOMER ATTEMPTED TO RESOLVE THE ISSUE BY TRYING MULTIPLE BATTERIES. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22501889 ↗MalfunctionJul 11, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT DURING ROUTINE CHECK, THE VIDEO LARYNGOSCOPE HAD NO DISPLAY. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22479217 ↗MalfunctionJul 8, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT PRIOR TO USAGE, THE VIDEO LARYNGOSCOPE'S SCREEN HAD NO DISPLAY, BUT LED LIGHT WAS ON. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22437757 ↗
Other LARYNGOSCOPE, RIGID devices
- McGRATH MAC 300-000-000Covidien LP · LARYNGOSCOPE, RIGID1 recall1 death205 reports
- n.a. 8404HXKarl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID242 reports
- McGRATH 340-000-000Covidien LP · LARYNGOSCOPE, RIGID2 deaths192 reports
- McGRATH MAC 301-000-000Covidien LP · LARYNGOSCOPE, RIGID2 recalls90 reports
- n.a. 8404BXCKarl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID141 reports
- n/a 8404AXCKarl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID108 reports
- McGRATH 340-000-000Covidien LP · LARYNGOSCOPE, RIGID84 reports
- GlideScope® GlideScope® Core™ 15 FHDVerathon Medical (Canada) ULC · Laryngoscope, Rigid1 recall30 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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