Use caution Medical device recall · FDA · Published January 15, 2025

DeRoyal AMG Suction Tubing Recall: Risk of Inadequate Suction in Patient Care

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1174-2025Medical device DeRoyal ›

Use caution until it’s fixed

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.

Take action

Contact the company

Recalling firmDeRoyal Industries Inc200 Debusk Ln · Powell, TN 37849-4703

✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/53082-deroyal-amg-suction-tubing-recall-risk-of-inadequate-suction-in.

Source Summary by GovInfoNow · govinfonow.com/recall/53082-deroyal-amg-suction-tubing-recall-risk-of-inadequate-suction-in · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1174-2025

Cite this page

“DeRoyal AMG Suction Tubing Recall: Risk of Inadequate Suction in Patient Care.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53082-deroyal-amg-suction-tubing-recall-risk-of-inadequate-suction-in. Based on FDA recall #Z-1174-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1174-2025%22&limit=1).

The FDA announced on Jan. 15, 2025, that DeRoyal Industries Inc is recalling DeRoyal AMG Suction Connector Tubing due to a potential seal failure that could cause inadequate suction and delay patient care. The voluntary Class II recall affects approximately 224,770 units distributed in the U.S. and Kuwait.

How to tell if you have it

Brand: DeRoyal
Product: AMG Suction Connector Tubing
REFs: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520
Lot Numbers: CNWKD04-01 through CNWKD04-10, CNWKD09-02, CNWKD09-08, CNWKD09-05, CNWKD09-07, CNWKD10-05, CNWKD10-06
Expiration Dates: 4/4/2029 through 10/12/2029

The hazard

The tubing may not ensure that the yankauer stays intact and secure to the tubing, resulting in a tight seal. This defect could result in inadequate suction and cause delay in patient care.

Context

GovInfoNow's records show DeRoyal Industries Inc has 29 other recalls on record since June 7, 2017. Other recent recalls of similar products include DeRoyal Suction Tubing Recall (Jan. 31, 2025), Medline Intubation Tray Recall (Dec. 24, 2025), and Medline 14 Fr Suction Catheter Kits Recall (Dec. 24, 2025).

How to tell if you have this one

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.

Brand
DeRoyal
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Tubing Model
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).
Verify Expiration Dates
Check the lot numbers and expiration dates listed in the recall notice for affected batches.

Where it went and when

Where it was distributed

Distributed in 21 states.

FDA distribution: “U.S.: ND, NY, VA, WV, NJ, TN, OK, TN, GA, OH, MN, AZ, WI, IL, MA, MD, MO, AR, MS, NY, MS, SC, HI, AR, UT, HI, O.U.S.: Kuwait” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, Arkansas, Georgia, Hawaii, Illinois, Maryland, Massachusetts, Minnesota, Mississippi, Missouri, New Jersey, New York, North Dakota, Ohio, Oklahoma, South Carolina, Tennessee, Utah, Virginia, West Virginia, Wisconsin.

Recall timeline

FDA published this recall 42 days after the firm started it.

Jan 15, 2025Firm started the recall
Feb 14, 2025FDA classified it Class II
Feb 26, 2025Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Keep exploring

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Link to this recall

<a href="https://govinfonow.com/recall/53082-deroyal-amg-suction-tubing-recall-risk-of-inadequate-suction-in">DeRoyal AMG Suction Tubing Recall: Risk of Inadequate Suction in Patient Care (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-1174-2025 (January 15, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1174-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.