Medline recalls kits containing B. Braun IV Administration Sets that may have stuck check valves, risking improper medication delivery. Affected kits have specific labels and lot numbers.
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 sets with a check valve that might get stuck open or closed. This could lead to incorrect medication delivery if the valve doesn't move properly.
The check valve in the administration sets might get stuck in either the open or closed position. This could prevent proper medication flow, leading to incorrect dosing or incomplete treatment.
Healthcare workers using these kits for patient medication administration are most at risk. Patients receiving IV treatments with these kits could experience medication errors.
Check for kits labeled 'AN01 CAROTID ANESTH KIT-LF' with Medline SKU PHS972096014B. Lot numbers starting with 25JMC398 are affected.
Look for the label 'AN01 CAROTID ANESTH KIT-LF' on the kit packaging.
Confirm the lot number starts with 25JMC398 to identify affected kits.
The check valve in the administration sets may become stuck open or closed, which could lead to incorrect medication delivery.
The recall record does not specify a remedy, so contact Medline directly for guidance.
Yes, patients receiving IV treatments with these kits could experience medication errors if the check valve gets stuck.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1049-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1049-2026 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.
