Merit Medical recalls custom tubing kits with serial numbers K04-00417, K04-00963, K04-01029 due to potential air trapping in medical lines that could affect patient safety.
High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.
Merit Medical is recalling specific custom tubing kits because high pressure tubing may relax over time, creating a void that traps air in the medical line. This trapped air could be introduced into the patient during use, posing a risk to their health.
The tubing may relax over time, creating a gap between the tubing and connector. This gap can trap air in the medical line, which might then be introduced into the patient during use, potentially causing health issues.
Patients using these custom tubing kits for medical purposes are at risk. Healthcare providers and medical device users who own the recalled kits should check their serial numbers.
Check the product reference numbers (K04-00417, K04-00963, K04-01029) on the tubing kit. The kits were sold with specific expiration dates and serial numbers listed in the recall notice.
Look for the reference numbers K04-00417, K04-00963, or K04-01029 on the tubing kit.
High pressure tubing may relax over time, creating a void that traps air in the medical line, which could be introduced into the patient during use.
Check for reference numbers K04-00417, K04-00963, or K04-01029 on the tubing kit.
The recall does not specify a remedy, so no action is required beyond checking if the product is affected.
We’ve drafted a message you can send Merit Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2294-2025 — Merit Medical Systems Merit Medical Systems Hello, I own a Merit Medical Systems that is covered by recall Z-2294-2025 from Merit Medical 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.
