DeRoyal AMG Suction Connector Tubing (REF: 71-2083, 71-C506, etc.) may not seal properly, causing delays in patient care. Affected units include specific lot numbers and expiration dates.
The tubing may not ensure that the yankauer stays intact, and secure to the tubing / yankauer connection for a tight seal. This could result in inadequate suction and cause delay in patient care.
DeRoyal AMG Suction Connector Tubing (model numbers 71-2083, 71-C506, 71-C510, 71-C512, 71-C520) is recalled because it may not seal tightly to the yankauer, risking delays in patient care. This is critical for medical use where proper suction is needed.
The tubing may not create a tight seal with the yankauer (suction device), leading to inadequate suction. This could cause delays in patient care, which is especially dangerous in medical emergencies where timely treatment is critical.
Healthcare professionals using this tubing for medical suction in patient care settings are most at risk. Patients relying on this equipment for critical medical procedures could experience delays in treatment.
Check for model numbers 71-2083, 71-C506, 71-C510, 71-C512, or 71-C520 on the tubing. Lot numbers and expiration dates are listed in the recall notice for specific batches.
Identify the model number on the tubing to see if it matches the recalled items (71-2083, 71-C506, 71-C510, 71-C512, 71-C520).
Check the lot numbers and expiration dates listed in the recall notice for affected batches.
The tubing may not seal tightly to the yankauer, which could cause inadequate suction and delay patient care in medical settings.
Model numbers 71-2083, 71-C506, 71-C510, 71-C512, and 71-C520 are affected.
Look for the model numbers listed above and check the lot numbers and expiration dates provided in the recall notice.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-1174-2025 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-1174-2025 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.
