Integra LifeSciences recalls MoniTorr CSF drainage systems due to reported stopcock breakage. Affected models include 10100, 10102, and others. Consumers should contact for remedy.
The firm has identified a complaint trend regarding breakage of the LimiTorr Transducer Mount stopcock and MoniTorr Panel Mount stopcock.
Integra LifeSciences is recalling several MoniTorr CSF drainage systems because stopcocks can break. This breakage could lead to leaks or infections in patients with brain or spinal fluid drainage systems.
The stopcocks in these drainage systems can break, potentially causing leaks or infections. This is a concern for patients with cerebrospinal fluid (CSF) drainage systems, as breaks could compromise the system's ability to safely manage fluid pressure.
Patients using MoniTorr CSF drainage systems for brain or spinal fluid management are most at risk. Healthcare providers who use these systems for medical treatments may also be affected.
Check for model numbers 10100, 10102, 10110, 10140, 10150, 10110A, SP0017, SP0042, SP0090, SP0164, or SP0236 on the product packaging or label. These systems were sold with the MoniTorr brand for CSF drainage.
Identify the model number on the product label or packaging to confirm if it is affected.
Reach out to Integra LifeSciences for instructions on how to return or replace the affected product.
Integra LifeSciences has identified a complaint trend regarding breakage of the stopcocks in these CSF drainage systems.
Affected models include MoniTorr 10100, 10102, 10110, 10140, 10150, 10110A, SP0017, SP0042, SP0090, SP0164, and SP0236.
Check the model number on the product label or packaging. Affected models are listed in the recall notice.
We’ve drafted a message you can send Integra LifeSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-1310-2019 — Integra LifeSciences Integra LifeSciences Hello, I own a Integra LifeSciences that is covered by recall Z-1310-2019 from Integra LifeSciences. 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.
