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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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High RiskFDA Device
Medical Devices

Medline Hudson RCI Oxygen Masks Recalled for Tubing Disconnection Risk

Agency Publication Date: January 8, 2026
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Summary

Medline Industries, LP has recalled approximately 1,611,081 Medline Hudson RCI Medium Concentration Oxygen Masks. The recall was initiated because the manufacturer received multiple complaints about the oxygen tubing disconnecting from the mask. If the tubing detaches during use, it can interrupt oxygen delivery, causing a delay in care and potentially leading to serious respiratory issues for the patient.

Risk

A detached tube can cause a patient to experience shortness of breath and hypoxia (dangerously low oxygen levels). These conditions may require emergency medical intervention to prevent the patient's breathing from deteriorating further.

What You Should Do

  1. This recall affects Medline Hudson RCI Medium Concentration Oxygen Masks with catalog numbers 1041CE, HUD1035, HUD1042, HUD1930, and HUDRHO41U.
  2. Check the catalog number and lot number printed on the product packaging. Because this recall affects a high volume of production batches, see the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled devices immediately. Contact Medline Industries, LP or your medical equipment distributor to arrange for a return, replacement, or correction.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for more information.

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: Medline Hudson RCI Medium Concentration Oxygen Masks
Model / REF:
1041CE
HUD1035
HUD1042
HUD1930
HUDRHO41U
Lot Numbers (224):
24DOA701
25EOA321
25EOA589
25EOA724
25EOA730
25EOA781
25EOA857
25FOA151
25FOA152
25FOA153
25FOA206
25FOA218
25FOA219
25FOA220
25FOA221
25FOA275
25FOA287
25FOA288
25FOA418
25FOA419
25FOA420
25FOA421
25FOA422
25FOA514
25FOA515
25FOA524
25FOA525
25FOA551
25FOA552
25FOA553
25FOA556
25FOA557
25FOA642
25FOA643
25FOA647
25FOA648
25FOA649
25FOA650
25FOA722
25FOA740
25FOA864
25FOA865
25FOA866
25GOA055
25GOA065
25GOA066
25GOA077
25GOA078
25GOA096
25GOA098
UDI:
00888277446727
40888277446725
10197344011575
20197344011572
10197344011544
20197344011541
10197344009626
20197344009623
10197344010646
20197344010643

Quantity: 1,611,081 eaches

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98125
Status: Active
Manufacturer: Medline Industries, LP
Sold By: Authorized medical device distributors; Healthcare facilities; Hospitals
Manufactured In: United States
Units Affected: 1,611,081 eaches
Distributed To: Nationwide

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.