Leucovorin Calcium for Injection, USP, 350 mg/vial, Rx only, labeled as a) Teva Parenteral Medicines, Inc., Irvine, CA…

Is this the product you have?

• Leucovorin Calcium for Injection, USP, 350 mg/vial, Rx only, labeled as a) Teva Parenteral Medicines, Inc., Irvine, CA 92618
• and b) Manufactured ByTeva Pharmaceuticals USA, Inc., North Wales, PA 19454, novaplus+, NDC 0703-5145-01

Lot codes and dates

• • Lot # a) 31324653B
  • exp. date 03/2021
  • 31326066B
  • exp. date 11/2021
  • 31326428B
  • exp. date 02/2022
  • 31327949B
  • exp. date 10/2022
  • 31327995B
  • exp. date 10/2022
  • 31328031B
  • exp. date 11/2022
  • 31328217B
  • exp. date 12/2022
  • 31328325B
  • exp. date 12/2022
  • 31328425B
  • exp. date 07/2021
  • Lot # b) 31324480B
  • exp. date 02/2021
  • Lot # 31327396B
  • exp. date 08/2022

Amount recalled

705,745 vials

This recall covers 15 products

The agency filed one notice per product. You are reading one of them; the other 14 are below.

• Dacarbazine for Injection USP, 200 mg, Single Use Vial (NDC 0703-5075-01), packaged in…
• Desmopressin Acetate Injection USP, 4 mcg/mL, 1 mL Preserved Vial (NDC 0703-5051-01)…
• Sterile Diluent for Epoprostenol Sodium for Injection, 50 mL vial (NDC 0703-9258-01)…
• Epoprostenol Sodium for Injection, 0.5 mg/vial (500,000 ng), 1X10ML vial, Rx only, Teva…
• MethyIPREDNISolone Acetate Injectable Suspension USP, 40 mg/mL, 1 mL Single-Dose Vial…
• Leucovorin Calcium for Injection, USP, 100 mg/vial, Single-Dose Vial, Rx only, Teva…
• Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 2 mL Single-Use Vial NDC…
• Toposar (etoposide injection USP), 1 gram/50 mL (20 mg/mL), 50 mL Multiple-dose Vial…
• Vecuronium Bromide for Injection, 10 mg, 1 mg/mL when reconstituted to 10 mL, 10 mL…
• Epoprostenol Sodium for Injection, 1.5 mg/vial (1,500,000 ng), 10 mL vial, Rx only…
• MethyIPREDNISolone Acetate Injectable Suspension USP, 80 mg/mL, 1 mL Single-Dose Vial…
• MethyIPREDNISolone Acetate Injectable Suspension USP, 400 mg/10 mL (40 mg/mL), 10 mL…

2 more are in the archive.

Where it was sold

• Nationwide
• PR

Why it was recalled

Lack of Assurance of Sterility: manufacturing areas for the recalled products exceeded acceptance levels for microbial recovery leading to a lack of sterility assurance for these sterile injectable products.

This product could cause temporary or reversible health problems — stop using it.