American Contract Systems recalls Convenience Kits CV B PACK (TNCB10AP) 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 Convenience Kits CV B PACK (model TNCB10AP) because samples of the catheters inside didn't meet performance standards. This could mean the catheters might not work properly, which could affect medical use.
The catheters in the kits may not meet required performance standards, which could lead to improper function during medical procedures. This might cause issues like incorrect placement or failure to deliver medication.
Healthcare professionals using these kits for catheter care are most likely affected. Patients receiving catheter care through these kits could be at risk if the catheters don't function as intended.
Check for the model number TNCB10AP on the kit. Units sold with lot code 42-8808611 and expiration date January 6, 2027 are affected.
Look for model number TNCB10AP, lot code 42-8808611, and expiration date January 6, 2027 on the kit.
Medline Industries identified that representative samples of the catheters in the kits 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 potential performance issues, but the record does not describe specific safety 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-3002-2026 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-3002-2026 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.
