Baxter recalls specific EXACTAMIX Inlet models due to incorrect labeling that may lead to expired product use. Affected lots include 802279, 802: 802280, 802281.
Specific lots of EXACTAMIX Inlets listed below due to incorrectly performed over-labeling. The inlets were over-labeled with a blank label, or with a label containing an extended expiration date. If the product is used beyond the expiration date,
Baxter is recalling specific lots of EXACTAMIX Inlets used in pharmacy compounding systems because they were incorrectly labeled with blank or extended expiration dates. Using these inlets after the expiration date could lead to unsafe medication preparation.
The inlets were over-labeled with blank labels or extended expiration dates. If used beyond the expiration date, this could result in expired medication solutions being prepared.
Pharmacists and pharmacy staff who use the EXACTAMIX 2400 Compounding System are most at risk. The affected lots are limited to specific production runs.
Check the lot number on the EXACTAMIX Inlet packaging. Affected lots are 802279, 802280, and 802281. These inlets are used with the Exacta-Mix 2400 Compounding System.
Look for the lot number on the EXACTAMIX Inlet packaging to determine if it is affected (802279, 802280, or 802281).
The inlets were over-labeled with blank labels or extended expiration dates, which could lead to using expired medication solutions.
Lots 802279, 802280, and 802281.
Check the lot number on the EXACTAMIX Inlet packaging; affected lots are 802279, 802280, and 802281.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1909-2018 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1909-2018 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.