Lanreotide Injection, 120 mg/0.5 mL, 0.5 mL per pre-filled syringe, For deep subcutaneous injection, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-870-67
Reported: January 21, 2026 Initiated: January 2, 2026 #D-0290-2026
Product Description
Lanreotide Injection, 120 mg/0.5 mL, 0.5 mL per pre-filled syringe, For deep subcutaneous injection, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-870-67
Reason for Recall
Presence of Particulate Matter.
Details
- Recalling Firm
- Cipla USA, Inc.
- Units Affected
- 15,221 syringes
- Distribution
- Nationwide in the USA
- Location
- Warren, NJ
Frequently Asked Questions
What product was recalled? ▼
Lanreotide Injection, 120 mg/0.5 mL, 0.5 mL per pre-filled syringe, For deep subcutaneous injection, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-870-67. Recalled by Cipla USA, Inc.. Units affected: 15,221 syringes.
Why was this product recalled? ▼
Presence of Particulate Matter.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 21, 2026. Severity: Moderate. Recall number: D-0290-2026.
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