Recall Z-0941-2022— MEDLINE INDUSTRIES, LP - Northfield
Class II · Ongoing
Class II FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2022-03-09. FDA's recall record names no specific 510(k) clearance for this event. Product: Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box. Reason: The mask cuff may disconnect from the device's breathing tube..
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-03-09
- Firm location
- Northfield, IL, United States
Product description
Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box
Reason for recall
The mask cuff may disconnect from the device's breathing tube.
Data sourced from openFDA. This site is unofficial and independent of the FDA.