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recall
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Sandoz Inc recall (Cls I)

July 9, 2025updated 5mo ago
community read0 votes

Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in Austria by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540, NDC: 0781-6136-94. — Reason: Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for Injection, USP, 20 million Unit — Status: Ongoing

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same company · ±60 days · 6

  • recallSandoz Inc recall (Cls I)Jul 9, 2025
  • approvalDIFLUPREDNATE: DUREZOL (DIFLUPREDNATE) — FDA approvalJul 15, 2025
  • approvalHYRIMOZ: HYRIMOZ (ADALIMUMAB-ADAZ) — FDA approvalJul 29, 2025
  • approvalMEDROL: METHYLPREDNISOLONE — FDA approvalAug 1, 2025
  • approvalMEDROL: METHYLPREDNISOLONE — FDA approvalAug 1, 2025
  • approvalMEDROL: METHYLPREDNISOLONE — FDA approvalAug 1, 2025

🐶 often sniffed alongside

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  • drugHYRIMOZ26 co-mentions · 13 sources
  • drugLarotid14 co-mentions · 7 sources
  • drugamoxicillin14 co-mentions · 7 sources
  • drugVOQUEZNA DUAL PAK14 co-mentions · 7 sources
  • drugAMOXICILLIN AND CLAVULANATE POTASSIUM14 co-mentions · 7 sources
  • drugVOQUEZNA TRIPLE PAK14 co-mentions · 7 sources
  • drugHUMIRA13 co-mentions · 13 sources

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