Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Family Medical Supply Compressed Oxygen Recalled for Quality Deviations

Agency Publication Date: November 16, 2023
Share:
Sign in to monitor this recall

Summary

Family Medical Supply Inc has recalled 26,657 cylinders of Compressed Oxygen USP (UN 1072) due to deviations from Current Good Manufacturing Practice (cGMP) quality standards. These cylinders, sold in various sizes including C, D, E, H, M, and M6, were manufactured and distributed between May 10, 2023, and October 31, 2023. While no injuries or incidents have been reported, the recall was initiated because the products may not meet the strict quality and purity standards required for medical oxygen.

Risk

Failure to follow quality standards during manufacturing can result in medical oxygen that does not meet safety or purity specifications. This could lead to a lack of effective treatment for patients who depend on these cylinders for respiratory support.

What You Should Do

  1. This recall affects Compressed Oxygen USP (UN 1072) packaged in cylinders labeled as Size C, D, E, H, M, and M6 under the Family Medical Supply brand, distributed from Dunn, North Carolina.
  2. Check your oxygen cylinders for manufacturing or distribution dates between May 10, 2023, and October 31, 2023.
  3. If you have health concerns regarding the use of this product, contact your healthcare provider or pharmacist immediately.
  4. Return any unused product to the place of purchase for a refund, throw it away, or contact Family Medical Supply Inc directly for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Oxygen, Compressed USP, UN 1072by Family Medical Supply
Variants: Size C, Size D, Size E, Size H, Size M, Size M6, Rx only
Date Ranges: Manufactured and distributed May 10, 2023, through October 31, 2023

Recall #: D-0106-2024; Total Quantity: 26,657 Cylinders.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93418
Status: Resolved
Manufacturer: Family Medical Supply Inc
Sold By: Family Medical Supply Inc
Manufactured In: United States
Units Affected: 26,657 Cylinders
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.