Drugs & medicalClass III

Pine Pharmaceuticals, LLC recalls Bevacizumab 2.5 mg/0.1 mL, Solution for Injection in 1mL, silicone free slip tip syringe, each Syringe supplied in individually labeled…

Labeling: Incorrect or Missing Lot and/or Exp Date: Lot code on primary packaging is incorrect.

Read the official notice →
Date
2023-04-19
Country
United States
Brand
Pine Pharmaceuticals
Product
Bevacizumab 2.5 mg/0.1 mL, Solution for Injection in 1mL, silicone free slip tip syringe, each Syringe supplied in individually labeled…
Classification
Class III
Units
Nationwide in the USA
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Pine Pharmaceuticals recalls

  1. 2023-10-25
  2. US
  3. 2023-01-11
  4. US
    Drugs & medicalClass II

    Pine Pharmaceuticals, LLC recalls Epi-Caine, Epinephrine 0.025% Lidocaine HCL 0.75% Solution for Intraocular Injection, 1 ml, Single Dose Vial, Compounded by Pine…

    CGMP Deviations: Raw material recalled by repackager, due to discoloration.

    FDA · DrugPine Pharmaceuticals, LLCNationwide to medical facilities.Official notice →
  5. 2022-09-21
  6. US
    Drugs & medicalClass II

    Pine Pharmaceuticals, LLC recalls Bupivacaine HCl 0.375% w/v and Lidocaine HCl 2% w/v Solution for Retrobulbar or Peribulbar Injection; packaged in a) 10 mL prefilled…

    Lack of Assurance of Sterility

    FDA · DrugPine Pharmaceuticals, LLCProduct was distributed to direct accounts in AL, CA, NC and NYOfficial notice →
All 4 Pine Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2023-04-19
  2. US
    Drugs & medicalClass I

    Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump, Model No. LVP-0004

    Fluid ingress that can cause a loss of electrical funtion and failure of the Set ID Sensory, resulting in the prevention of infusion or halt of infusion.

    FDA · DeviceFresenius Kabi USA, LLCDomestic: CA, CO, NJ, WI, & UT. No foreign distribution.Official notice →
  3. US
    Drugs & medicalClass III

    Focus Health Group Inc recalls Epinephrine Professional EMS, Epinephrine Convenience Kit, Epinephrine 1 mg/mL, Rx Only, Focus Health Group, Manufactured for: Focus…

    Labeling; Incorrect NDC number on outer carton of product.

    FDA · DrugFocus Health Group IncNationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass III

    Pfizer Inc. recalls MEKTOVI (binimetinib) tablets, 15 mg, 180-count bottle, Rx only, Distributed by: Array BioPharma Inc., a wholly owned subsidiary of Pfizer…

    Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle labels state an expiry date of March 2026; the correct expiration date is February 2025.

    FDA · DrugPfizer Inc.Nationwide in the USAOfficial notice →
  5. US
  6. US
    Drugs & medicalClass III

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Norepinephrine Bitartrate Injection, USP, 4 mg/4 mL* (1 mg/mL), 4 mL Single-dose Fliptop Vial (NDC 47335-615-40); packaged in…

    Failed Impurities/Degradation Specifications: Above the specification limits yielded for related substance norepinephrine sulfonic acid impurity during routine product monitoring.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide in the USAOfficial notice →
  7. 2023-04-12
  8. US
    Drugs & medicalClass II

    Abbott Molecular, Inc. recalls Abbott Alinity m System, REF 08N53-002, containing Amplification Detetction Unit (ADU) #4.

    The instrument was found to be installed without plunger assemblies in the clamp bar for an Amplification Detection Unit. After correction of the issue, the instrument was returned for use without calibration. This…

    FDA · DeviceAbbott Molecular, Inc.US Distribution to state of: PA, a government account.Official notice →
See all drugs & medical recalls →