DYNJ 60792C, 61157C, 61168D, 61740D, 67835, 80849B, 80849J, 84653A, 900904J, 900904K, 900904L, 900904M, 902585, 902585A, 908393, 908393A, 909573, 910384, 910384A, 390015M
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
DYNJ 60792C, 61157C, 61168D, 61740D, 67835, 80849B, 80849J, 84653A, 900904J, 900904K, 900904L, 900904M, 902585, 902585A, 908393, 908393A, 909573, 910384, 910384A, 390015M
No specific danger
All
Check for proper labeling and ensure the product is within its expiration date
Check the product label for the correct lot number and expiration date.
Ensure the product is within its expiration date.
Contact the manufacturer if there are any concerns about the product.
DYNJ products are medical devices manufactured by Medline Industries, LP.
DYNJ products are generally safe when used as intended and within their expiration dates.
Check the product label for the correct lot number and expiration date.
We’ve drafted a message you can send DYNJ to request your refund or repair — edit it as you like.
Subject: Recall Z-1413-2026 — DYNJ DYNJ Hello, I own a DYNJ that is covered by recall Z-1413-2026 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.
