Cook recalls Rupsch-Uchida Transjugular Liver Access Sets (RUPS-100) due to potential incorrect manufacturing length. Affected units may not be properly trimmed or inspected, risking procedure complications.
Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.
Cook is recalling certain liver access sets used in medical procedures because they might have been made to the wrong length or not properly trimmed. This could lead to complications during medical procedures if the sets are used.
The recalled sets may have been cut to the incorrect length or not properly trimmed during manufacturing. This could cause improper fit during medical procedures, potentially leading to complications.
Healthcare professionals using these liver access sets in medical procedures are most at risk. Patients undergoing specific liver-related procedures may be affected if the recalled sets are used.
Check for reference part number RUPS-100. The product was sold with order number G06929 and lot number 16659065. These sets are used in transjugular liver procedures.
Verify the reference part number and lot number on the device to confirm if it is affected.
Cook identified that some units may have been manufactured out of specification, potentially being cut to the wrong length or not properly trimmed.
The recall does not specify a remedy, so check the product details to see if it matches the affected lot numbers.
The recall indicates potential complications during medical procedures if the sets are used, but no specific injuries have been reported.
We’ve drafted a message you can send Cook to request your refund or repair — edit it as you like.
Subject: Recall Z-0995-2026 — Cook Cook Hello, I own a Cook that is covered by recall Z-0995-2026 from Cook. 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.
