Home / Recalls / Fresenius Kabi Compounding, LLC / D-0015-2025

D-0015-2025 Class II Terminated

Recalled by Fresenius Kabi Compounding, LLC — Canton, MA

Recall Details

Product Type
Drugs
Report Date
October 30, 2024
Initiation Date
September 25, 2024
Termination Date
August 15, 2025
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1631 bags

Product Description

Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 20 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC 71506-024-58

Reason for Recall

cGMP violations

Distribution Pattern

Product was distributed to 125 direct accounts nationwide.

Code Information

Lot # C274-000037046, exp. date 13-Oct-24

Other recalls by Fresenius Kabi Compounding, LLC

  • D-0337-2026 Class II — vancomycin HCl, 2 grams, 2 grams added to 500 mL, 0.9% Sodium Chloride Injection (February 5, 2026)
  • D-0333-2026 Class II — acyclovir sodium, 200 mg, 200mg added to 100 mL, 0.9% Sodium Chloride Injection, (February 5, 2026)
  • D-0335-2026 Class II — thiamine HCl, 500 mg, 500 mg added to 100 mL, 0.9% Sodium Chloride Injection, US (February 5, 2026)
  • D-0336-2026 Class II — vancomycin HCl, 1.5 grams, 1.5 grams added to 500 mL, 0.9% Sodium Chloride Injec (February 5, 2026)
  • D-0334-2026 Class II — ketamine HCl, 1,000 mg, 1,000 mg per 100 mL (10 mg per mL) in Sodium Chloride In (February 5, 2026)
  • D-0016-2025 Class II — Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 10 mg per 250 mL, Single D (September 25, 2024)
  • D-0020-2025 Class II — NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP, 8 mg per 250 mL, S (September 25, 2024)
  • D-0021-2025 Class II — Oxytocin 0.9% Sodium Chloride Injection USP, 30 units per 500 mL Single Dose Bag (September 25, 2024)
  • D-0019-2025 Class II — NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP, 4 mg per 250 mL, S (September 25, 2024)
  • D-0014-2025 Class II — Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 20 mg per 250 mL, Single D (September 25, 2024)