HIGHRegulatoryTier 1

American Regent, Inc. Issues Voluntary Nationwide Recall of One Lot of Papaverine Hydrochloride Injection, USP 60 mg/ 2 mL Due to the Presence of Visible Particulate Matter

SourceFDA RecallsTier 1Hard News

By FDA

Originally at fda.gov

Summary & scoring by The Bell Brief (Dr. Jennifer Bell) using the Drill-Down Protocol (Drill-Down Score) — not the original publisher.

Why it matters for dental

Dental practices that stock Papaverine HCl Injection (used for priapism emergencies or off-label vascular procedures) face a recall of Lot 24072, removing a critical medication from the crash cart and exposing clinics to both patient-safety risk and potential liability if the particulate-laden vials are inadvertently administered.

Key points

  • Lot 24072 of 60 mg/2 mL single-dose vials is being pulled nationwide because visible glass particles were detected.
  • Recall is at the consumer level, so any dental office that purchased this lot must quarantine stock and return it immediately.
  • Papaverine is occasionally kept in oral-surgery or implant suites for managing acute priapism or for intra-arterial vasodilation; loss of this vial could delay emergency response.
  • No other lots or sizes of Papaverine HCl Injection are included in this recall, allowing offices to verify stock numbers before re-ordering.

Who should care

OwnerAssociateSpecialist

Read the original on FDA Recalls

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