Recall Z-0948-2022— Baxter Healthcare Corporation
Class II · Terminated
Class II FDA medical device recall by Baxter Healthcare Corporation, initiated 2022-02-25, terminated 2026-03-02. FDA's recall record names no specific 510(k) clearance for this event. Product: Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.. Reason: Product is mislabeled as self-righting Luer slip tip caps, yellow..
- Recalling firm
- Baxter Healthcare Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2022-02-25
- Terminated
- 2026-03-02
- Firm location
- Deerfield, IL, United States
Product description
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
Reason for recall
Product is mislabeled as self-righting Luer slip tip caps, yellow.
Data sourced from openFDA. This site is unofficial and independent of the FDA.