Recall Z-1227-2015— Baxter Corporation Englewood
Class II · Terminated
Class II FDA medical device recall by Baxter Corporation Englewood, initiated 2014-12-29, terminated 2016-08-08. FDA's recall record names no specific 510(k) clearance for this event. Product: Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93866025, H93867025, H93867100, H938671025, H938671100, H938673025, H938673100, H938674025, H938674100, H938676025, H938676100, H938677025, H938677100, H938679025, H938679100, H938690025, H93869025, H938693025, H938696025, H93868025, H93868100, H938672025, H938672100, H938675025, H938675100, H938678025, and H938678100.. Reason: Self-Righting Luer Tip Caps were manufactured and shipped with a missing latex symbol on both single and case labels..
- Recalling firm
- Baxter Corporation Englewood
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-12-29
- Terminated
- 2016-08-08
- Firm location
- Englewood, CO, United States
Product description
Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93866025, H93867025, H93867100, H938671025, H938671100, H938673025, H938673100, H938674025, H938674100, H938676025, H938676100, H938677025, H938677100, H938679025, H938679100, H938690025, H93869025, H938693025, H938696025, H93868025, H93868100, H938672025, H938672100, H938675025, H938675100, H938678025, and H938678100.
Reason for recall
Self-Righting Luer Tip Caps were manufactured and shipped with a missing latex symbol on both single and case labels.
Data sourced from openFDA. This site is unofficial and independent of the FDA.