Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Baxter Recalled by Baxter Corporation Englewood Due to Self-Righting Luer Tip Caps were manufactured and shipped...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Corporation Englewood directly.
Affected Products
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.
Quantity: 1,404,230
Why Was This Recalled?
Self-Righting Luer Tip Caps were manufactured and shipped with a missing latex symbol on both single and case labels.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Baxter Corporation Englewood
Baxter Corporation Englewood has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report