Recall Z-1288-2022— Baxter Healthcare Corporation
Class II · Ongoing
Class II FDA medical device recall by Baxter Healthcare Corporation, initiated 2022-05-17. FDA's recall record names no specific 510(k) clearance for this event. Product: #1 MAC F/O LARYNGOSCOPE; F/O Laryngoscope Set-MAC; F/O Laryngoscope Set-MAC W/LED. Reason: Packaging error..
- Recalling firm
- Baxter Healthcare Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-05-17
- Firm location
- Deerfield, IL, United States
Product description
#1 MAC F/O LARYNGOSCOPE; F/O Laryngoscope Set-MAC; F/O Laryngoscope Set-MAC W/LED
Reason for recall
Packaging error.
Data sourced from openFDA. This site is unofficial and independent of the FDA.