Baxter recalls specific EXACTAMIX Inlet lots (802284-802286) due to over-labeling with blank or extended expiration dates. Using expired product may cause safety issues. Affected pharmacy users should check their lot numbers.
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 (802284-802686) because they were over-labeled with blank labels or extended expiration dates. Using these inlets after the expiration date could lead to expired product use, which may cause safety risks in pharmacy compounding.
The inlets were over-labeled with blank labels or labels showing extended expiration dates. If used beyond the expiration date, the product could expire, potentially causing safety issues in pharmacy compounding.
Pharmacists and pharmacy staff using the EXACTAMIX 2400 Compounding System are most at risk. The affected lots are specific to the inlets used in pharmacy compounding.
Check the lot number on the EXACTAMIX Inlet packaging. The affected lots are 802284, 802285, and 802286. These inlets are part of the Exacta-Mix 2400 Compounding System used in pharmacies.
Look for the lot number on the EXACTAMIX Inlet packaging. Affected lots are 802284, 802285, and 802286.
Baxter EXACTAMIX Inlets (lot numbers 802284, 802285, 802286) used in the Exacta-Mix 2400 Compounding System for pharmacy compounding.
The inlets were over-labeled with blank labels or labels showing extended expiration dates, which could lead to using expired product.
Check the lot number on the packaging. If it's 802284, 802285, or 802286, stop using it and contact Baxter for guidance.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1911-2018 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1911-2018 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.
