FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

Tailstorm Health Bevacizumab Recall

BEVACIZUMAB (AVASTIN)1

Tailstorm Health INC · Phoenix, AZ

Risk level
Class II
Reported by FDA
Nov 27, 2024
Recall ID
D-0051-2025
Check your lot numberHow we source this data

Summary

Tailstorm Health recalled Bevacizumab starting Nov 6, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0051-2025 on Nov 27, 2024. Reason: Lack of Sterility Assurance. Status: Terminated.

Why it was recalled

Lack of Sterility Assurance

Product description

BEVACIZUMAB (AVASTIN)1.25mg/0.05mL, Sterile Injection, 0.5 mL Single-Dose Syringe, Rx Only, Repackaged by: Medivant Healthcare: 24416 N 19th Ave, Phoenix, AZ, NDC 81483-0041-1

Lot numbers, UPCs & expiration codes

Lot #: D24005, Exp. Date 20 February 2025; D24006, Exp. Date 21 February 2025; D24007, Exp. Date 22 February 2025; D24008, Exp. Date 19 March 2025; D24009, Exp. Date 20 March 2025; D24012, Exp. Date 25 April 2025.

Where it was sold

Nationwide Within U.S.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0051-2025
Classification
Class II
Status
Terminated
Recall initiated
Nov 6, 2024
FDA report date
Nov 27, 2024
Quantity
27,560 Syringes
Recall type
Voluntary: Firm initiated
Recalling firm
Tailstorm Health INC

Original FDA data

Every field from FDA enforcement report D-0051-2025, exactly as published.

Show all FDA fields
City
Phoenix
State
AZ
Status
Terminated
Country
United States
Event ID
95718
Address
24416 N 19th Ave Ste 200
Code information
Lot #: D24005, Exp. Date 20 February 2025; D24006, Exp. Date 21 February 2025; D24007, Exp. Date 22 February 2025; D24008, Exp. Date 19 March 2025; D24009, Exp. Date 20 March 2025; D24012, Exp. Date 25 April 2025.
Postal code
85085-1400
Report date
Nov 27, 2024
Product type
Drugs
Recall number
D-0051-2025
Classification
Class II
Recalling firm
Tailstorm Health INC
Product quantity
27,560 Syringes
Termination date
Mar 28, 2025
Reason for recall
Lack of Sterility Assurance
Voluntary / mandated
Voluntary: Firm initiated
Product description
BEVACIZUMAB (AVASTIN)1.25mg/0.05mL, Sterile Injection, 0.5 mL Single-Dose Syringe, Rx Only, Repackaged by: Medivant Healthcare: 24416 N 19th Ave, Phoenix, AZ, NDC 81483-0041-1
Distribution pattern
Nationwide Within U.S.
Recall initiation date
Nov 6, 2024
Initial firm notification
Letter
Center classification date
Nov 18, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0051-2025, published Nov 27, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

How we source and update recall data · Report incorrect information

Other recent drug recalls