American Contract Systems recalls Convenience Kit CV B PACK (Model TNCB10AN) due to catheters not meeting performance specs. Affected units sold until Jan 2027.
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 (Model TNCB10AN) because samples of the catheters inside didn't meet safety performance standards. This could mean the catheters might not work properly, potentially causing injury during medical use.
The catheters in the kit were found to not meet required performance standards. This could mean they might not function correctly during medical procedures, potentially causing injury if used improperly.
Healthcare workers using the kit for catheter procedures and patients receiving care through this kit are likely affected. Those with the specific model number and lot code are at risk.
Check for the model number TNCB10AN on the kit. The lot code 42-8768511 and expiration date of January 6, 2027 are also on the kit.
Look for model number TNCB10AN, lot code 42-8768511, and expiration date January 6, 2027 on the kit.
Medline Industries, LP 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 recall indicates the catheters may not meet performance standards, but the record does not specify injury risks.
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-3001-2026 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-3001-2026 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.
