Smiths Medical ASD Inc.: Device Recall
Recall #Z-0143-2025 · 07/18/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0143-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Smiths Medical ASD Inc.
- Status
- Ongoing
- Date Initiated
- 07/18/2024
- Location
- Minneapolis, MN, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 251,591 units
Reason for Recall
Uncertainty in the seal integrity of the sterile packaging.
Product Description
smiths medical portex, Nasopharyngeal Airway, Sizes as follows: a) AIRWAY NASOPHARYNGEAL 6.0MM, REF 100/210/060; b) AIRWAY NASOPHARYNGEAL 6.0MM, REF 100/210/060JP; c) AIRWAY NASOPHARYNGEAL 7.0MM, REF 100/210/070; d) AIRWAY NASOPHARYNGEAL 7.0MM, REF 100/210/070JP; e) AIRWAY NASOPHARYNGEAL 8.0MM, REF 100/210/080; f) AIRWAY NASOPHARYNGEAL 8.0MM, REF 100/210/080JP; g) AIRWAY NASOPHARYNGEAL 8.0MM, REF 100/210/080JS; h) AIRWAY NASOPHARYNGEAL 9.0MM, REF 100/210/090; i) AIRWAY NASOPHARYNGEAL 9.0MM, REF 100/210/090JP;
Distribution Pattern
Worldwide distribution.
Other Recalls by Smiths Medical ASD Inc.
- Class I: Dangerous 04/10/2025
- Class I: Dangerous 04/10/2025
- Class I: Dangerous 04/10/2025
- Class I: Dangerous 04/10/2025
- Class I: Dangerous 04/10/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.