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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

Remington Medical, Inc.: Remington Medical Drainage Bags Recalled for Labeling Errors

Agency Publication Date: December 5, 2023
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Summary

Remington Medical, Inc. has recalled approximately 3,080 Medical Drainage Bags (Model REF 600-D) because the packaging labels contain incorrect information regarding the product's manufacturing date and expiration date. Consumers who rely on these labels may use a product that is potentially past its shelf life or not be able to accurately track the device's age. These drainage bags were distributed specifically to locations in Pennsylvania and Florida.

Risk

Incorrect manufacturing and expiration dates on the label can lead to the use of a medical device beyond its intended lifespan, which may compromise the sterility or structural integrity of the drainage bag. This could potentially increase the risk of infection or device failure during medical procedures.

What You Should Do

  1. Locate the Remington MEDICAL Drainage Bag box and check the label for Model REF 600-D and Lot Number 2325111.
  2. Verify the Unique Device Identifier (UDI/DI) number 20813079020008 printed on the packaging to confirm if your product is part of this recall.
  3. If your product matches these identifiers, contact your healthcare provider or Remington Medical, Inc. at 6830 Meadowridge Ct, Alpharetta, Georgia, 30005-2202, to determine if the product is safe for continued use or to arrange for a replacement.
  4. Healthcare facilities should immediately quarantine any affected stock to prevent the distribution of incorrectly labeled units.
  5. For additional information or questions regarding this recall, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA).

Your Remedy Options

๐Ÿ“‹Other Action

Contact for guidance

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Remington MEDICAL Drainage Bag, REF 600-D
Model / REF:
600-D
UPC Codes:
20813079020008
Lot Numbers:
2325111

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93377
Status: Active
Manufacturer: Remington Medical, Inc.
Sold By: authorized medical distributors
Manufactured In: United States
Units Affected: 3080 devices
Distributed To: Pennsylvania, Florida

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.