DeRoyal recalls specific polyurethane feeding tubes due to connector detachment risk. Affected models include REF 54-2450R, 54-2465R, 54-2480R, and 54-3680R with certain lot numbers. No remedy is stated in the recall notice.
Certain MED-RX Polyurethane Feeding Tubes are being recalled due to a product concern where the connector has detached from the feeding tube.
DeRoyal is recalling specific polyurethane feeding tubes because the connector can detach from the tube. This poses a risk of the tube becoming dislodged during use, which could lead to injury or complications for patients needing feeding assistance.
The connector can detach from the feeding tube during use, potentially causing the tube to become dislodged. This could lead to the tube being pulled out of the body or causing injury to the patient. The risk is higher for patients who require ongoing tube feeding.
Patients using enteral feeding tubes and caregivers who own the recalled models. Those most at risk are individuals with medical conditions requiring tube feeding who may experience injury if the tube detaches.
Check for the model numbers REF 54-2450R, 54-2465R, 54-2480R, or 54-3680R on the tube packaging. The specific lot numbers listed in the recall notice (e.g., 142844, 142843) also indicate affected units.
Identify the model number and lot number on the feeding tube to determine if it is recalled.
The recall notice does not specify any remedy or action steps for affected users.
The affected models are REF 54-2450R, 54-2465R, 54-2480R, and 54-3680R with specific lot numbers listed in the recall notice.
The connector can detach from the feeding tube during use, potentially causing the tube to become dislodged and leading to injury or complications.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-2293-2019 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-2293-2019 from DeRoyal. 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.
