Baxter recalls yellow self-righting syringe tip caps due to potential sterile barrier failure. Affected packs include 25 and 100-packs with specific reference numbers. Consumers should check their product details and contact Baxter for guidance.
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Baxter is recalling yellow self-righting syringe tip caps that may not maintain a sterile barrier. This could lead to contamination of medical devices during use, posing a risk to patients receiving injections.
The packaging might not keep the tip caps sterile, which could contaminate medical devices during use. This risk occurs when the caps are exposed to air or moisture, potentially leading to infections.
Healthcare professionals and patients using Baxter DISCPAC Syringe Tip Caps for injections. Those with the specific reference numbers listed in the recall are most at risk.
Check for the yellow color, self-righting design, and Luer slip connection. Affected packs have reference numbers H93866025, H93866100, or H938690025 with specific UDI codes.
Look for the reference numbers H93866025, H93866100, or H938690025 on the packaging.
The packaging may not maintain a sterile barrier for the tip caps, which could lead to contamination during medical use.
Check the reference numbers on the packaging. If you have the affected models, contact Baxter for further instructions.
The recall addresses potential contamination, not direct injury risks. The hazard level is low risk.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1575-2022 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1575-2022 from Baxter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
