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🏥 FDA: McKesson — Class I

healthcarebearishSource: FDA
90%Confidence
0Views
FDASource
2026-03-03Date

Summary

McKesson faces a Class I recall for UDENYCA due to temperature abuse, indicating potential supply chain quality control failures. This could impact patient safety and regulatory compliance for Accord BioPharma's product distribution.

Actionable: Monitor McKesson's supply chain practices and consider reviewing contracts with Accord BioPharma for compliance risks.

AI Confidence: 90%

Data Points

firmMcKesson
classificationClass I
statusOngoing
distributionNationwide in the USA
productUDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe, Rx only, Manufactured by Accord BioPharma, Inc., 8041 Arco Corporate

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