Class II · Moderate risk
Zoledronic Acid Injection 5mg/100mL Sterile Solution
Lack of Assurance of Sterility: Leaking vials
National Drug Code
Is NDC 55111-0688-52 recalled?
Zoledronic Acid · 100 mL in 1 BOTTLE, GLASS (55111-688-52)
Yes — this exact package was recalled
3 FDA recalls name the code 55111-0688-52 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Zoledronic Acid
- Strength
- ZOLEDRONIC ACID 5 mg/100mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Dr.Reddy's Laboratories Ltd
- Type
- Human Prescription Drug
- Product code
- 55111-0688
Recalls naming this package
Class III · Low risk
Zoledronic Acid Injection
Failed Impurities/Degradation Specifications: OOS for unknown impurities.
Class II · Moderate risk
Zoledronic Acid Injection
Lack of Assurance of Sterility; defective seals where the metal silver ring was not attached tightly to the vial
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 55111-0121 Atorvastatin Calcium 4
- 55111-0123 Atorvastatin Calcium 4
- 55111-0180 Tizanidine 4
- 55111-0136 Zenatane 3
- 55111-0179 Tizanidine 3
- 55111-0320 Glimepiride 3
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