Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported December 10, 2014
McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items, each individually peel-pouched and EtO sterilized. Product Usage: Single Use, sterile video laryngoscope blade for use with McGRATH MAC Video Laryngoscopes
The blade retaining clip may be difficult to engage and thereby increase the possibility of a blade becoming disconnected during intubation, specifically when the device is being…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Aircraft Medical Limited recalled McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items, each indiv… - a moderate-severity action.
McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items, each indiv… was recalled by Aircraft Medical Limited in December 10, 2014. Reason: The blade retaining clip may be difficult to engage and thereby increase the possibility of a blade becoming…. Check the official notice for the remedy. Verify recall #Z-0494-2015 with the FDA Devices before acting.
The recall
Aircraft Medical Limited issued this moderate-severity FDA Devices recall-The blade retaining clip may be difficult to engage and thereby increase the possibility of a blade becoming….
- Moderate
- severity level
- Class II
- classification
- December 10, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0494-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0494-2015) was formally reported on December 10, 2014, with the manufacturer initiating the action on November 4, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Aircraft Medical Limited is listed as the recalling firm, operating out of EDINBURGH, N/A. Federal records list the affected scope as 40,900 blades (US); 16,000 blades (Foreign).
The documented reason for this recall is: The blade retaining clip may be difficult to engage and thereby increase the possibility of a blade becoming disconnected during intubation, specifically when the device is being retracted from the patients mouth. Distribution data in the federal record shows the product reached: Worldwide Distribution - US Nationwide in the state of GA and the countries of Austria, China, Denmark, Finland, France, Hong Kong, Israel, Italy, Netherlands, Poland, Saudi Arabia, Singapore, South Korea, Taiwan, and T…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
40,900 blades (US); 16,000 blades (Foreign)
Related Recalls
6
3 from same agency
Product description
McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items, each individually peel-pouched and EtO sterilized. Product Usage: Single Use, sterile video laryngoscope blade for use with McGRATH MAC Video Laryngoscopes
Reason for recall
The blade retaining clip may be difficult to engage and thereby increase the possibility of a blade becoming disconnected during intubation, specifically when the device is being retracted from the patients mouth.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0494-2015 |
| Date reported | December 10, 2014 |
| Date initiated | November 4, 2014 |
| Recalling firm | Aircraft Medical Limited |
| Firm location | EDINBURGH, N/A |
| Affected scope | 40,900 blades (US); 16,000 blades (Foreign) |
| Distribution | Worldwide Distribution - US Nationwide in the state of GA and the countries of Austria, China, Denmark, Finland, France, Hong Kong, Israel, Italy, Netherlands, Poland, Saudi Arabia, Singapore, South Korea, Taiwan, and Turkey. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0494-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items, each individually peel-pouched and EtO sterilized. Product Usage: Single Use, sterile video laryngoscope blade for use with McGRATH MAC Video Laryngoscopes. Recalled by Aircraft Medical Limited. Units affected: 40,900 blades (US); 16,000 blades (Foreign).
Why was this product recalled? ▼
The blade retaining clip may be difficult to engage and thereby increase the possibility of a blade becoming disconnected during intubation, specifically when the device is being retracted from the patients mouth.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 10, 2014. Severity: Moderate. Recall number: Z-0494-2015.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution - US Nationwide in the state of GA and the countries of Austria, China, Denmark, Finland, France, Hong Kong, Israel, Italy, Netherlands, Poland, Saudi Arabia, Singapore, South Korea, Taiwan, and Turkey..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0494-2015) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported December 10, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.