Baxter recalls dark blue self-righting syringe tip caps due to potential failure to maintain sterile packaging. Affected products include 25-packs and 100-packs with specific reference numbers. Consumers should check their packaging details to determine if they are affected.
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Baxter is recalling dark blue self-righting syringe tip caps that may not maintain a sterile barrier. This could lead to contamination of medical devices during use. Affected products include specific 25-packs and 100-packs with reference numbers.
The packaging may not maintain a sterile barrier, which could allow contamination of the syringe tips. This poses a risk of infection if the tips are used without proper sterility.
Healthcare professionals and patients using Baxter DISCPAC syringe tip caps for medical injections. Those with the specific reference numbers listed in the recall are most at risk.
Check for dark blue self-righting syringe tip caps with reference numbers H938693025 (25-packs) or H938673100 (100-packs). All lots of these products are affected.
Look for reference numbers H938693025 (25-packs) or H938673100 (100-packs) on the packaging.
The recall states there is a potential for the packaging not maintaining a sterile barrier, so they may not be safe for medical use.
The recall does not specify a remedy, so check the product details to see if you are affected and contact Baxter for further instructions.
Look for dark blue self-righting syringe tip caps with reference numbers H938693025 (25-packs) or H938673100 (100-packs).
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1578-2022 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1578-2022 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.
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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.
