American Contract Systems recalls Convenience Kit CV B PACK (TNCB10AM) due to catheters not meeting performance specs. Affected units sold through specific channels until 7/15/2026.
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable performance specifications.
American Contract Systems is recalling their Convenience Kit CV B PACK (TNCB10AM) because samples of the catheters inside didn't meet required performance standards. This could mean the catheters might not work properly, potentially causing issues during medical use.
The catheters in the kit may not meet required performance specifications, which could lead to improper function during medical procedures. This might cause issues like incorrect placement or failure to deliver medication as needed.
Healthcare professionals using the kit are most likely affected. Patients using these catheters could be at risk if the product doesn't function as intended.
Check for the model number TNCB10AM on the kit. The kit was sold with lot code 42-8493811 and expires July 15, 2026.
Look for the model number TNCB10AM on the kit label.
Medline Industries identified that representative samples of the catheters in the kit did not meet applicable performance specifications.
The recall record does not specify a remedy, so check with American Contract Systems for guidance.
The kit was sold with an expiration date of July 15, 2026.
We’ve drafted a message you can send American Contract Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-3000-2026 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-3000-2026 from American Contract Systems. 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.