Medline recalls two procedure kits with connectors that might not allow catheters to be inserted properly if not fully open. Affected kits have specific model numbers and lot numbers listed in the recall notice.
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Medline is recalling two procedure kits that have connectors which might not allow catheters to be inserted correctly if the connector isn't fully open. This could lead to improper catheter insertion during medical procedures.
The connectors in these procedure kits might not stay fully open, which could prevent catheters from being inserted as intended. This might lead to improper catheter placement during medical procedures.
Healthcare professionals using Medline procedure kits for catheter insertion are most at risk. Patients receiving catheter procedures using these kits may be affected.
Check for the model numbers DYNJRA9043S (ECHOSTIM BLOCK SET) or PAIN1622A (ULTRASOUND BLOCK PREP TRAY) on the kit. Lot numbers listed in the recall include 23CBE390 through 23IBG611 for the first kit and 21ELA821 through 23HLA896 for the second.
Look for model numbers DYNJRA9043S or PAIN1622A on the procedure kit.
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
The recall does not specify a remedy, so check with Medline directly for instructions.
Yes, the recall lists specific lot numbers for both kits: 23CBE390 through 23IBG611 for the first kit and 21ELA821 through 23HLA896 for the second.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0511-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0511-2025 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.
