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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

Fagron Sterile bevacizumab (Avastin) Injection Recalled for Sterility Concerns

Agency Publication Date: September 12, 2025
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Summary

Fagron Compounding Services is recalling approximately 109,320 syringes of bevacizumab (Avastin) Injection, 1.25mg/0.05mL (0.12 mL Fill). The recall was initiated because of a lack of assurance of sterility, which means the product may not be completely free of microorganisms. These sterile single-dose syringes are used as injections, often for ophthalmic or oncological conditions, and were distributed nationwide in the United States.

Risk

A lack of sterility in an injectable medication poses a significant risk of infection to the patient. If a contaminated product is injected, it can cause serious illness or permanent injury, particularly if injected into sensitive areas like the eye.

What You Should Do

  1. Stop using the recalled product immediately.
  2. Check the lot number and expiration date on the syringe label or outer packaging. Affected lot numbers include C274-000044756, C274-000044832, C274-000045387, and many others with expiration dates ranging from August to December 2025. See the Affected Products section below for the full list of affected codes.
  3. Contact Fagron Compounding Services or your distributor to arrange for the return of any unused syringes.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions or to report adverse events.

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 (Avastin) Injection, 1.25mg/0.05mL (0.12 mL Fill)by Fagron Sterile Services
Variants: Sterile Single-Dose Syringe
Lot Numbers (52):
C274-000044756 (Exp 8-30-2025)
C274-000044757 (Exp 8-30-2025)
C274-000044832 (Exp 9-4-2025)
C274-000044833 (Exp 9-4-2025)
C274-000044882 (Exp 9-6-2025)
C274-000044883 (Exp 9-6-2025)
C274-000044972 (Exp 9-8-2025)
C274-000045004 (Exp 9-18-2025)
C274-000045005 (Exp 9-18-2025)
C274-000045108 (Exp 9-13-2025)
C274-000045109 (Exp 9-13-2025)
C274-000045136 (Exp 9-14-2025)
C274-000045137 (Exp 9-14-2025)
C274-000045289 (Exp 9-20-2025)
C274-000045290 (Exp 9-20-2025)
C274-000045350 (Exp 9-22-2025)
C274-000045351 (Exp 9-22-2025)
C274-000045387 (Exp 9-25-2025)
C274-000045388 (Exp 9-25-2025)
C274-000045516 (Exp 9-27-2025)
C274-000045517 (Exp 9-27-2025)
C274-000045586 (Exp 10-2-2025)
C274-000045587 (Exp 10-2-2025)
C274-000045676 (Exp 10-4-2025)
C274-000045677 (Exp 10-4-2025)
C274-000045707 (Exp 10-5-2025)
C274-000045708 (Exp 10-5-2025)
C274-000045754 (Exp 10-9-2025)
C274-000045755 (Exp 10-9-2025)
C274-000045840 (Exp 10-11-2025)
C274-000045841 (Exp 10-11-2025)
C274-000046048 (Exp 10-24-2025)
C274-000046049 (Exp 10-24-2025)
C274-000046095 (Exp 10-25-2025)
C274-000046096 (Exp 10-25-2025)
C274-000046122 (Exp 10-26-2025)
C274-000046123 (Exp 10-26-2025)
C274-000046164 (Exp 10-30-2025)
C274-000046165 (Exp 10-30-2025)
C274-000046191 (Exp 10-31-2025)
C274-000046192 (Exp 10-31-2025)
C274-000046240 (Exp 11-1-2025)
C274-000046241 (Exp 11-1-2025)
C274-000046315 (Exp 11-6-2025)
C274-000046316 (Exp 11-6-2025)
C274-000046345 (Exp 11-7-2025)
C274-000046346 (Exp 11-7-2025)
C274-000046515 (Exp 11-14-2025)
C274-000046516 (Exp 11-14-2025)
C274-000046603 (Exp 11-16-2025)

Manufactured by Fagron Sterile Services, 8710 E 34th St N. Wichita, KS 67226.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97540
Status: Active
Manufacturer: Fagron Compounding Services
Sold By: Hospitals; Surgical Centers; Infusion Centers; Wholesalers
Manufactured In: United States
Units Affected: 109,320 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.