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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

DeRoyal Suction Connector Tubing Recalled for Potential Suction Failure

Agency Publication Date: March 5, 2025
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Summary

DeRoyal Industries Inc is recalling approximately 714 cases of Suction Connector Tubing because the tubing connector is too small to fit properly onto medical suction canisters. This size issue, combined with the hardness of the plastic, makes it difficult to connect the tubing to the canister lid, which can result in inadequate suction or a delay in patient care during medical procedures. No incidents or injuries have been reported at this time.

Risk

The inner diameter of the tubing connector is too narrow for standard suction canister ports, preventing a secure connection and potentially leading to a loss of suction during fluid removal procedures.

What You Should Do

  1. This recall affects DeRoyal Suction Connector Tubing (Reference numbers 71-C5100NS, 71-C6100NS, and 71-C7100NS) used for medical fluid movement.
  2. Identify the affected products by checking the packaging for UDI-DI codes 00749756578738, 00749756578851, or 00749756578967.
  3. Confirm if your product is affected by checking for lot numbers CNWKD04-04, CNWKD04-05, CNWKD04-10, CNWKD09-08, CNWKD04-06, or CNWKD04-07.
  4. Stop using the recalled device immediately.
  5. Contact DeRoyal Industries Inc or your medical distributor to arrange for the return, replacement, or correction of the tubing.
  6. Call the FDA at 1-888-463-6332 for additional questions regarding this medical device recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: DeRoyal Suction Connector Tubing
Model / REF:
71-C5100NS
71-C6100NS
71-C7100NS
Lot Numbers:
CNWKD04-04
CNWKD04-05
CNWKD04-10
CNWKD09-08
CNWKD04-06
CNWKD04-07
UDI:
00749756578738
00749756578851
00749756578967

Quantity affected: 714 cases. Indicated use: Fluid Movement.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96261
Status: Active
Manufacturer: DeRoyal Industries Inc
Sold By: medical distributors
Manufactured In: United States
Units Affected: 714 cases
Distributed To: Illinois, Minnesota, North Carolina, Pennsylvania, Virginia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.