Solus Flexible Laryngeal Mask Airway
Solus Flexible Laryngeal Mask Airway Recall Solus Flexible Laryngeal Mask Airway devices are being recalled in Canada because the mask cuff may not seal properly during use, potentially allowing anesthetic gases to leak and patient secretions to enter the airway. This recall affects all Solus devices distributed across Canada. The device is a medical airway tool used during anesthesia and surgery.
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-06-05
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/e9ff7c0a-0444-4152-9960-6508f91c244c