Carefusion recalls Thora-Para 8 Fr Catheter Drainage Tray without lidocaine due to potential air leaks that could cause patient complications. Learn if your product is affected and what to do.
The Universal Drainage Set (UDS) may contain valves that leak internally which may result in the introduction of up to 30cc of air into the patient.
Carefusion is recalling Thora-:Para 8 Fr Catheter Drainage Trays without lidocaine because they may leak internally, introducing up to 30cc of air into patients. This could lead to complications like increased pressure in the body.
The drainage tray may have internal valves that leak, allowing up to 30cc of air to enter the patient's system. This air can increase pressure in the body, potentially causing complications during medical procedures.
Patients using this drainage tray for medical procedures are at risk. Healthcare providers who use the product for catheter drainage systems are most affected.
Check for the product name 'Thora-Para 8 Fr Catheter Drainage Tray w/o Lidocaine' with catalog number TPT1000CDF and UDI 50885403231900. The batch number is 0001333309.
Identify if your tray has the catalog number TPT1000CDF and UDI 50885403231900 with batch 0001333309.
The recall states the drainage tray may leak internally, introducing air that could cause complications. It is not safe to use without checking if it's affected.
The recall does not specify a remedy, so check the product details to see if it's affected. If it is, contact Carefusion for further instructions.
Look for the catalog number TPT1000CDF and UDI 50885403231900 with batch 0001333309.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2654-2020 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-2654-2020 from Carefusion. 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.
