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Class II: temporary or reversible health riskOngoing

Dr. Reddy's Laboratories Zoledronic Acid Injection 5mg/100mL Sterile Recall

Zoledronic Acid Injection 5mg/100mL Sterile Solution, 100mL Single-Dose vials, Rx only,…

Dr. Reddy's Laboratories, Inc. · Princeton, NJ

Risk level
Class II
Reported by FDA
Jun 5, 2024
Recall ID
D-0510-2024
Check your lot numberHow we source this data

Summary

Dr. Reddy's Laboratories recalled Zoledronic Acid Injection 5mg/100mL Sterile starting May 23, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0510-2024 on Jun 5, 2024. Reason: Lack of Assurance of Sterility: Leaking vials. Status: Ongoing.

Why it was recalled

Lack of Assurance of Sterility: Leaking vials

Product description

Zoledronic Acid Injection 5mg/100mL Sterile Solution, 100mL Single-Dose vials, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-688-52

Lot numbers, UPCs & expiration codes

Lot #: G3000010, Exp. Date 11/2025

Where it was sold

Nationwide within the United States

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-0510-2024
Classification
Class II
Status
Ongoing
Recall initiated
May 23, 2024
FDA report date
Jun 5, 2024
Quantity
13,880 vials
Recall type
Voluntary: Firm initiated
Recalling firm
Dr. Reddy's Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report D-0510-2024, exactly as published.

Show all FDA fields
City
Princeton
State
NJ
Status
Ongoing
Country
United States
Event ID
94686
Address
107 College Rd E
Code information
Lot #: G3000010, Exp. Date 11/2025
Postal code
08540-6623
Report date
Jun 5, 2024
Product type
Drugs
Recall number
D-0510-2024
Classification
Class II
Recalling firm
Dr. Reddy's Laboratories, Inc.
Product quantity
13,880 vials
Reason for recall
Lack of Assurance of Sterility: Leaking vials
Voluntary / mandated
Voluntary: Firm initiated
Product description
Zoledronic Acid Injection 5mg/100mL Sterile Solution, 100mL Single-Dose vials, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-688-52
Distribution pattern
Nationwide within the United States
Recall initiation date
May 23, 2024
Initial firm notification
Letter
Center classification date
May 28, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0510-2024, published Jun 5, 2024. View the source record (openFDA) · FDA enforcement reports

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

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