Integra LifeSciences recalls LimiTorr CSF drainage systems due to potential stopcock breakage. This could lead to improper drainage and infection risks. Affected models include INS9020 and INS9030 series. Contact for return instructions.
The firm has identified a complaint trend regarding breakage of the LimiTorr Transducer Mount stopcock and MoniTorr Panel Mount stopcock.
Integra LifeSciences is recalling LimiTorr CSF drainage systems because the stopcocks may break, potentially causing improper drainage and infection risks. This affects patients using these systems for brain or spinal fluid drainage.
The stopcocks in the LimiTorr system can break, which may lead to improper drainage of cerebrospinal fluid. This could cause infections or other complications if the system is not functioning correctly.
Patients using LimiTorr CSF drainage systems for brain or spinal fluid management are most at risk. The recall applies to all units sold, including specific model numbers.
Check for model numbers like INS9020, INS9020SP1, INS9030, or INS9030SP1 on the product label. The product is used for draining cerebrospinal fluid from the brain or spinal area.
Look for model numbers such as INS9020, INS9020SP1, INS9030, or INS9030SP1 on the device label.
Reach out to Integra LifeSciences for specific return or repair instructions.
The recall is due to a complaint trend about breakage of the stopcocks in the LimiTorr Transducer Mount and MoniTorr Panel Mount components.
The affected models include INS9020, INS9020SP1, INS9030, and INS9030SP1.
The recall states a potential for improper drainage and infection risks, but does not specify serious injury in normal use.
We’ve drafted a message you can send Integra LifeSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-1312-2019 — Integra LifeSciences Integra LifeSciences Hello, I own a Integra LifeSciences that is covered by recall Z-1312-2019 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.
