Baxter recalls EXACTAMIX Inlet (H938173) for particulate matter in pharmaceutical compounding devices. Affected units include specific lot numbers and product codes. Consumers should check their units and contact Baxter for details.
Baxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H938174, H938175, H938176, used with the ExactaMix and ExactaMix Pro compounders. Particulate matter has been observed within the inlet primary packaging inlet components, including within the sterile fluid path tubing, before use.
Baxter is recalling EXACTAMIX Inlet components due to observed particulate matter in the sterile fluid path tubing. This could contaminate pharmaceutical compounds, posing a risk to patient safety during compounding.
Particulate matter has been found inside the sterile fluid path tubing of the inlets before use. This could lead to contamination of compounded medications, potentially affecting patient safety.
Pharmaceutical compounding professionals using Baxter EXACTAMIX Inlets with ExactaMix or ExactaMix Pro compounders are most at risk. Affected units include specific product codes and lot numbers.
Check for product codes H938173, H938174, H938175, or H938176 on the inlet. Affected units have lot numbers 803806 and lower. The inlets are used with ExactaMix or ExactaMix Pro compounders.
Look for product codes H938173, H938174, H938175, or H938176 on the inlet.
Confirm the lot number is 803806 or lower to determine if the unit is affected.
Particulate matter has been observed in the sterile fluid path tubing before use, which could contaminate compounded medications.
Check for product codes H938173, H938174, H938175, or H938176 and lot numbers 803806 or lower.
The recall does not require immediate stop use; affected units should be checked and contacted for further instructions.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-3082-2024 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-3082-2024 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.
