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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/Surgical Equipment

Centurion Circumcision Kits Recalled for Lack of Sterility

Agency Publication Date: April 16, 2026
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Summary

Medline Industries, LP is recalling 640 Centurion Circumcision Kits because one production lot was distributed without undergoing the required sterilization process. These kits, which are intended for surgical use, are not sterile and could cause serious infections. The affected kits (Medline Kit Number CIT7050F) were distributed to healthcare facilities in South Carolina and are identified by Lot Number 25KLA002.

Risk

Using a non-sterile circumcision kit during a surgical procedure introduces bacteria and other pathogens directly into a surgical site, posing a high risk of serious infection to the patient.

What You Should Do

  1. Identify your product by checking for Centurion Circumcision Kit (Medline Kit Number/SKU CIT7050F) with Lot Number 25KLA002.
  2. Check the packaging for UDI/DI 10198459536656 (each) or 40198459536657 (case).
  3. Stop using the recalled product immediately.
  4. Contact Medline Industries, LP or your distributor to arrange for the return, replacement, or correction of the affected kits.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions.

Your Remedy Options

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

Affected Products

Product: CENTURION Circumcision Kit
Model / REF:
CIT7050F
Lot Numbers:
25KLA002
UDI:
10198459536656
40198459536657

Distributed in South Carolina.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98626
Status: Active
Manufacturer: Medline Industries, LP
Sold By: Nationwide distribution
Manufactured In: United States
Units Affected: 640
Distributed To: South Carolina

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.