Baxter recalls sterile 5mL oral dispensers with mislabeled product codes and volumes. Affected units may have incorrect labeling that could lead to improper use.
Affected lot of 5 mL oral dispensers was packaged in individual pouches that are mislabeled with the incorrect product code (H93876101) and volume (1mL).
Baxter Healthcare is recalling sterile EXACTAMED Oral Dispensers that were mislabeled with the wrong product code and volume. This could lead to users administering the wrong amount of medication.
The dispensers were packaged with incorrect product codes and volume labels. This could lead to users administering the wrong amount of medication, potentially causing improper dosing.
People who own or use the recalled sterile EXACTAMED Oral Dispensers with product code H93876105. Those using the dispensers for medication administration are most at risk.
Check for the product code H93876105 on the dispenser. The affected units were sold with lot number 1203395 and expire by November 30, 2019.
Look for the product code H93876105 on the dispenser's label.
The affected lot of dispensers was mislabeled with the incorrect product code (H93876101) and volume (1mL) instead of 5mL.
The recall record does not specify a remedy, so no action is required beyond checking the label.
The recall indicates potential mislabeling that could lead to improper dosing, but the dispenser itself is not unsafe if used correctly.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0806-2018 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-0806-2018 from Baxter Healthcare. 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.