Medline recalls kits with B. Braun IV Administration Sets and Pump Administration Sets labeled DR HOLCOMB FACIAL due to check valve components potentially getting stuck, which could affect safe use.
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
Medline is recalling kits that include B. Braun IV Administration Sets and Pump Administration Sets labeled 'DR HOLCOMB FACIAL' because the check valve might get stuck open or closed. This could lead to improper medication delivery if the valve doesn't function correctly.
The check valve in the IV sets might get stuck in either the open or closed position. This could prevent proper medication flow or cause incorrect dosing if the valve doesn't move as intended.
Healthcare workers using these kits for patient medication administration are most at risk. Patients receiving IV treatments with these kits could be affected if the check valve malfunctions.
Look for kits labeled 'DR HOLCOMB FACIAL' with the Medline SKU DYNJ54488A. The lot number 25HBQ850 or UDI/DI numbers 10193489587869 (EA) and 40193489587860 (CS) indicate the recalled items.
Look for the label 'DR HOLCOMB FACIAL' on the kit to identify if it's part of the recall.
Reach out to Medline directly for guidance on next steps if you have the recalled kit.
The check valve components may become stuck in the open or closed positions, which could affect medication delivery.
Check the label for 'DR HOLCOMB FACIAL' and contact Medline for further instructions.
Yes, if the check valve gets stuck, it could prevent proper medication flow or cause incorrect dosing.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1054-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1054-2026 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.
