Recall Z-2401-2021— Smiths Medical ASD Inc.
Class II · Terminated
Class II FDA medical device recall by Smiths Medical ASD Inc., initiated 2021-08-04, terminated 2025-03-11. FDA's recall record names no specific 510(k) clearance for this event. Product: smiths medical portex Tracheal Intubation Stylet, REF 100/120/200, 4.0mm OD X 335mm, 10/box, sterile.. Reason: The incorrect device is contained in the package..
- Recalling firm
- Smiths Medical ASD Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-08-04
- Terminated
- 2025-03-11
- Firm location
- Minneapolis, MN, United States
Product description
smiths medical portex Tracheal Intubation Stylet, REF 100/120/200, 4.0mm OD X 335mm, 10/box, sterile.
Reason for recall
The incorrect device is contained in the package.
Data sourced from openFDA. This site is unofficial and independent of the FDA.