EPINEPHrine 8mg/250ml added to dextrose 5%, 32 mcg/mL, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200…

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• EPINEPHrine 8mg/250ml added to dextrose 5%, 32 mcg/mL, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043
• NDC72196-7019-1

Lot codes and dates

• Lot
  • 36-240224
  • Exp. 7/16/2023
  • 36-242322
  • EXP. 7/24/2023
  • 36-242445
  • Exp. 7/25/2023
  • 36-243305
  • Exp. 7/27/2023
  • 36-243813
  • Exp. 7/31/2023
  • 36-246166
  • 36-246167
  • Exp. 8/3/2023
  • 36-247670
  • Exp. 8/9/2023
  • 36-248992
  • Exp.8/16/2023
  • 36-249468
  • Exp. 8/17/2023
  • 36-249590
  • Exp.8/18/2023
  • 36-251336
  • 36-251644
  • Exp. 8/27/2023
  • 36-251461
  • Exp. 8/28/2023
  • 36-255531
  • 36-255532
  • Exp. 9/7/2023

Amount recalled

4,570 bags

This recall covers 95 products

The agency filed one notice per product. You are reading one of them; the other 94 are below.

• rocuronium50 mg/5 mL (10 mg/mL), Syringes Rx only, this drug was repackaged by CAPS…
• vancomycin 1 g/250 mL added to 0.9% sodium chloride, 4 mg/mL, IV Bag, Rx only, Cental…
• succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only, this drug was repackaged by…
• vancomycin 1.25 g/250 mL added to dextrose 5%, 5 mg/mL, IV Bag, Rx only, Central…
• dilTIAZem 125mg/125mL (1 mg/mL), added to dextrose 5%, IV Bag, RX only, Central…
• glycopyrrolate 1 mg/5 mL (0.2 mg/mL), For Anesthesia Use, Syringe, RX ONLY, CAPS, Inc.…
• dilTIAZem 125mg/125mL (1 mg/mL), added to 0.9% sodium chloride, IV Bag, Rx Only…
• EPINEPHrine 4mg/250mL added to 0.9% sodium chloride, IV Bag, RX only, Central Admixture…
• vancomycin 1.25 g/250 mL added to 0.9% Sodium Chloride, 5 mg/mL, IV Bag, Rx only…
• Cardioplegia Solution del Nido Formula, IV Bag, Total Volume = 1,052.8 mL, FOR…
• EPINEPHrine, 2 mg added to dextrose 5% 250mL, Concentration = 8 mcg/mL, IV Bag, Rx…
• EPINEPHrine added to dextrose 5%, 4mg/250ml, IV Bag, Rx Only, Central Admixture…

82 more are in the archive.

Where it was sold

• Nationwide

Why it was recalled

Lack of assurance of sterility. Validation data for decontamination cycles is lacking.

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