DYNJ - UDI/DI 10193489395907 (each), 40193489395908 (case) - Lot Number 22DBN952
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
DYNJ - UDI/DI 10193489395907 (each), 40193489395908 (case) - Lot Number 22DBN952
No known danger
All
Check for UDI/DI 10193489395907 (each), 40193489395908 (case) - Lot Number 22DBN952
Look for UDI/DI 10193489395907 (each), 40193489395908 (case) - Lot Number 22DBN952
UDI/DI 10193489395907 (each), 40193489395908 (case)
22DBN952
We’ve drafted a message you can send DYNJ to request your refund or repair — edit it as you like.
Subject: Recall Z-2493-2026 — DYNJ DYNJ Hello, I own a DYNJ that is covered by recall Z-2493-2026 from DYNJ. 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.
