Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Bevacizumab 2.5 mg/0.1 mL Recalled by Pine Pharmaceuticals, LLC Due to Labeling: Incorrect or Missing Lot and/or Exp Date:...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Pine Pharmaceuticals, LLC directly.
Affected Products
Bevacizumab 2.5 mg/0.1 mL, Solution for Injection in 1mL, silicone free slip tip syringe, each Syringe supplied in individually labeled poly envelopes (primary packaging). Repackaged by Pine Pharmaceuticals, Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150, Office Use Only, Not for Resale. Secondary packaging consists of a coated cardboard box, with order-specific label indicating lot number housed within order/container. NDC # 69194-0458-1
Quantity: 932 syringes
Why Was This Recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date: Lot code on primary packaging is incorrect.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Pine Pharmaceuticals, LLC
Pine Pharmaceuticals, LLC has 24 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report