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

Avella of Deer Valley, Inc. Store 38: Bevacizumab Pre-filled Syringes Recalled for Lack of Sterility Assurance

Agency Publication Date: November 7, 2018
Share:
Sign in to monitor this recall

Summary

Avella Specialty Pharmacy is recalling 911 units of Bevacizumab 2.5 mg/0.1mL pre-filled syringes (deliverable dose of 1.25mg in a Normject syringe) because they may not be sterile. The lack of sterility assurance in an injectable drug can lead to serious health complications or infections. These repackaged syringes were distributed nationwide and include NDC 42852-001-24 with a specific lot number and beyond-use date. Consumers should contact their healthcare provider or pharmacist immediately to determine if they received this medication and to discuss next steps.

Risk

If a drug intended for injection lacks assurance of sterility, it may contain microorganisms that can cause severe infections or life-threatening inflammatory responses when administered.

What You Should Do

  1. Check your medical records or medication packaging for Bevacizumab 2.5 mg/0.1mL pre-filled syringes (NDC 42852-001-24) repackaged by Avella Specialty Pharmacy.
  2. Verify if your product matches Lot # 138-20182408@58 with a Beyond Use Date (BUD) of 12/22/2018.
  3. Contact your healthcare provider or pharmacist immediately if you believe you have received or were treated with an affected syringe.
  4. Return any unused product to the pharmacy where it was purchased for a refund.
  5. Contact Avella of Deer Valley, Inc. Store 38 at their Phoenix, Arizona location for further instructions regarding this recall.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Refund for unused product

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: BEVACIZUMAB 2.5 MG/0.1ML, pre-filled syringe (deliverable dose of 1.25MG)
Model:
NDC 42852-001-24
Lot Numbers:
138-20182408@58 (BUD 12/22/2018)
138-20182408
Date Ranges: 12/22/2018 (Beyond Use Date)

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 81466
Status: Resolved
Manufacturer: Avella of Deer Valley, Inc. Store 38
Sold By: Avella Specialty Pharmacy
Manufactured In: United States
Units Affected: 911 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.