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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 Drug
Medications & Supplements/Prescription Drugs

Bevacizumab Intravitreal Syringes Recalled for Sterility Issues

Agency Publication Date: October 6, 2025
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Summary

RC Outsourcing, LLC is recalling 2,669 Bevacizumab (1.75 mg/0.07 mL) intravitreal syringes due to a lack of assurance of sterility. This medication is typically administered as an injection into the eye by a healthcare professional in a hospital or office setting. The recall affects syringes with four specific lot numbers and beyond-use dates (BUD) ranging from October 6 to October 20, 2025.

Risk

A lack of sterility assurance in an injectable eye medication poses a serious risk of infection or inflammation within the eye, which can lead to vision loss or other severe complications. No specific injuries have been reported to date.

What You Should Do

  1. Identify the affected products by checking for Bevacizumab 1.75 mg/0.07 mL syringes (0.07 mL Total Volume) labeled for 'Hospital/Office Use Only' from RC Outsourcing LLC.
  2. Verify the following lot numbers and Beyond-Use Dates (BUD) on the syringe packaging: 20250708-768A26 (BUD: Oct 06, 2025), 20250715-944DF2 (BUD: Oct 13, 2025), 20250722-55C603 (BUD: Oct 20, 2025), or 20250722-5DC113 (BUD: Oct 20, 2025).
  3. Stop using the recalled product immediately.
  4. Contact RC Outsourcing, LLC or your distributor to arrange for the return of any unused syringes.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) 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.

Affected Products

Product: Bevacizumab 1.75 mg/0.07 mL - 0.25 mL syringe
Variants: Intravitreal, 0.07 mL Total Volume
Lot Numbers:
20250708-768A26 (BUD: Oct 06, 2025)
20250715-944DF2 (BUD: Oct 13, 2025)
20250722-55C603 (BUD: Oct 20, 2025)
20250722-5DC113 (BUD: Oct 20, 2025)

Quantity: 2,669 syringes; Label includes: Rx Only, Hospital/Office Use Only, Refrigerate, RC Outsourcing LLC, Lowellville, OH 44436.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97653
Status: Resolved
Manufacturer: RC Outsourcing, LLC
Sold By: Hospitals; Physician Offices
Manufactured In: United States
Units Affected: 2,669 syringes
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.