OFFICIAL-SOURCE RECALL · AUSTRALIA
McGRATH MAC video laryngoscope Recall: Classification Class I Reason for the Action
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- McGRATH MAC video laryngoscope
- Manufacturer
- See official notice
- Lot number
- numbers
- Batch number
- numbers
- Serial number / range
- numbers
- Date code
- dates
- Expiration date
- dates
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
Classification Class I Reason for the Action Medtronic have reported that the battery management system within the devices being removed (McGRATH MAC EMS Video Laryngoscope device, catalogue number 300-200-000; supplied under Stryker Catalogue number 11996-000393) is not sufficient to mitigate against depletion of the battery voltage below the design threshold. Batteries that are depleted below the design threshold may increase the risk of the battery becoming unstable, which may lead to a thermal event followed by a risk of explosion. Instructions for Customers/Users Customers are to: - Immediately discontinue use of devices being removed. - Uninstall and dispose of the battery assembly from the device/s - A refund will be issued by Stryker for any affected devices on hand once the completed Response Form has been returned to postmarketssp@strkyer.com. Action Commencement Date 30/07/2026 Responsible Entity Stryker Australia Pty Ltd
Hazard
Classification Class I Reason for the Action Medtronic have reported that the battery management system within the devices being removed (McGRATH MAC EMS Video Laryngoscope device, catalogue number 300-200-000; supplied under Stryker Catalogue number 11996-000393) is not sufficient to mitigate against depletion of the battery voltage below the design threshold. Batteries that are depleted below the design threshold may increase the risk of the battery becoming unstable, which may lead to a thermal event followed by a risk of explosion. Instructions for Customers/Users Customers are to: - Immediately discontinue use of devices being removed. - Uninstall and dispose of the battery assembly from the device/s - A refund will be issued by Stryker for any affected devices on hand once the completed Response Form has been returned to postmarketssp@strkyer.com. Action Commencement Date 30/07/2026 Responsible Entity Stryker Australia Pty Ltd
Official recall notice
McGRATH MAC video laryngoscope
Agency: Therapeutic Goods Administration
Official publication date: July 26, 2024
Read the official AU_TGA_DRAC recall notice →Scan products you own
Scan products you own once and let RecallGuard monitor future official recalls.
Scan & Monitor Products