International safety notice
As a result of an investigation by overseas manufacturers, the products subject to this voluntary recall (McGRATH MAC video laryngoscope, product numbers 300-000-000, 300-200- 000) is insufficient to control battery voltage consumption that exceeds the design threshold. It turned out to be a minute. If the battery is depleted to We will carry out a voluntary collection of numbers.
Japan / PMDA Recalls · JPN · Jul 29, 2024
Key facts
| Title | As a result of an investigation by overseas manufacturers, the products subject to this voluntary recall (McGRATH MAC video laryngoscope, product numbers 300-000-000, 300-200- 000) is insufficient to control battery voltage consumption that exceeds the design threshold. It turned out to be a minute. If the battery is depleted to We will carry out a voluntary collection of numbers. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Hodor laryngoscope for rigid intubation Brand name: McGRATH MAC Video Laryngoscope |
| Manufacturer | Covidien Japan Co., Ltd. |
| Models | 388750, 374029, 388786, 370937, 373152, 374012, 398871, 371893, 396577, 399035, 401075, 397838 and 3761 more |
| Date | Jul 29, 2024 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1