Baxter recalls specific EXACTAMIX Inlet models due to incorrect labeling that may lead to expired product use. Affected lot numbers include 802277-802385. Contact for replacement.
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 certain EXACTAMIX Inlet components used in pharmacy compounding systems because they were incorrectly labeled with blank or extended expiration dates. Using these inlets beyond their expiration date could lead to unsafe medication preparation.
The inlets were over-labeled with blank labels or labels showing extended expiration dates. If used past the expiration date, this could result in expired medication solutions being prepared.
Pharmacists and pharmacy technicians who use the Exacta-Mix 2400 Compounding System with the recalled inlets are most at risk. The specific lot numbers listed in the recall affect these users.
Check the lot number on the EXACTAMIX Inlet packaging. Affected lots are 802277, 802278, 802383, 802384, and 802385. These inlets are part of the Exacta-Mix 2400 Compounding System.
Identify the lot number on the EXACTAMIX Inlet packaging to determine if it is one of the affected lots: 802277, 802278, 802383, 802384, or 802385.
Baxter EXACTAMIX Inlet, Non-Vented, High-Volume Inlet, REF H938173 used in the Exacta-Mix 2400 Compounding System.
Lot numbers 802277, 802278, 802383, 802384, and 802385.
Check the lot number on the EXACTAMIX Inlet packaging. Affected lots are 802277, 802278, 802383, 802384, and 802385.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1908-2018 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1908-2018 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.
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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.
