Medline recalls spinal and epidural procedure kits with specific model numbers due to connectors that may not allow catheters to be inserted as intended if not fully open.
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Medline is recalling spinal and epidural procedure kits that have connectors which might not allow catheters to be inserted properly if the connector isn't fully open. This could lead to improper catheter insertion during medical procedures.
The connectors in these kits may not stay in the fully open position, which can prevent catheters from being inserted as intended during medical procedures. This could lead to improper catheter placement.
Healthcare professionals using Medline procedure kits with the listed model numbers and lot codes are most at risk. Patients receiving these procedures may be affected if the kits are used incorrectly.
Check the product label for model numbers like DYNJRA1268B, DYNJRA1268C, or PAIN1845. Also look for lot numbers such as 20FLA512 or 22GLA287 on the packaging.
Look for model numbers and lot numbers on the product label to determine if it's recalled.
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Check the product label for model numbers like DYNJRA1268B, DYNJRA1268C, or PAIN1845, and lot numbers such as 20FLA512 or 22GLA287.
No action is required if the connector is in the fully open position. However, ensure proper use to avoid improper catheter insertion.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0509-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0509-2025 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.
