Baxter recalls green self-righting syringe tip caps due to potential failure to maintain sterile packaging. Affected packs have specific reference numbers and lot codes. Consumers should check their product details.
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Baxter is recalling green self-righting syringe tip caps that may not maintain sterile packaging. This could lead to contamination of medical devices during use, posing a risk to patient safety.
The packaging may not maintain a sterile barrier, which could allow contamination of the syringe tip caps. This might lead to infections or other complications if the caps are used in medical procedures without proper sterility.
Healthcare professionals and patients using Baxter DISCPAC Syringe Tip Caps for medical injections. Those with the specific reference numbers and lot codes listed in the recall are most at risk.
Check for the green color, self-righting design, and Luer slip connection. Affected packs have reference numbers: H93869025 (25 pack), H938674100 (100 pack), or H93869100 (100 pack).
Identify the reference number and lot code on the packaging to confirm if your item is affected.
The packaging may not maintain a sterile barrier, which could lead to contamination of the syringe tip caps during medical use.
The recall does not specify a remedy, so check the product details to confirm if it is affected and contact Baxter for further instructions.
Look for the green color, self-righting design, and Luer slip connection. Affected packs have reference numbers: H93869025 (25 pack), H938674100 (100 pack), or H93869100 (100 pack).
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1579-2022 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1579-2022 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.
