Recall Z-1581-2022— Baxter Healthcare Corporation
Class II · Ongoing
Class II FDA medical device recall by Baxter Healthcare Corporation, initiated 2022-07-22. FDA's recall record names no specific 510(k) clearance for this event. Product: Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Purple, 100 pack, REF H938677100. Reason: There is a potential of the packaging not maintaining a sterile barrier for the tip caps..
- Recalling firm
- Baxter Healthcare Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-07-22
- Firm location
- Deerfield, IL, United States
Product description
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Purple, 100 pack, REF H938677100
Reason for recall
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Data sourced from openFDA. This site is unofficial and independent of the FDA.