Medline recalls fluid delivery sets with white macro drip chambers that deliver three times more fluid per drop than required micro chambers, risking incorrect medication dosing.
Fluid Delivery Sets were incorrectly assembled with a white macro drip chamber instead of the required grey micro drip chamber. The macro drip chamber delivers three times more fluid per drop than the micro drip chamber.
Medline is recalling fluid delivery sets that were incorrectly assembled with a white macro drip chamber instead of the required grey micro drip chamber. This causes the set to deliver three times more fluid per drop than intended, which could lead to incorrect medication dosing.
The macro drip chamber delivers three times more fluid per drop than the micro chamber. This means medication could be delivered in larger quantities than intended, potentially causing overdose or incorrect dosing.
Healthcare professionals using the recalled fluid delivery sets for medication administration are most at risk. Patients receiving medication through these sets could receive incorrect dosages.
Look for the item number 99000069 or 949000221-224 with a white macro drip chamber. The sets were sold with lot numbers starting with 0000128741 through 0000139596.
Inspect the drip chamber for a white macro chamber instead of the required grey micro chamber.
The fluid delivery sets were incorrectly assembled with a white macro drip chamber instead of the required grey micro drip chamber.
The macro drip chamber delivers three times more fluid per drop than the micro chamber, which could lead to incorrect medication dosing.
Look for item numbers 99000069 or 949000221-224 with a white macro drip chamber and lot numbers starting with 0000128741 through 0000139596.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0764-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0764-2025 from Medline. 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.
