FDA Drug recall D-0254-2015

Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured b…

• FDA Drug
• Class III
• terminated
• Published 2014-11-26

On 2014-11-26 the FDA classified a Class III recall of Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured b… by Hospira, citing correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.

Read the official FDA Drug notice

Product

Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured by Hospira, Inc. Lake Forest, IL 60045, NDC 0409-6533-01.

Reason

Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.

Identifiers

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Other recalls by Hospira

• Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use Single-dose Syringe per carton, Rx only, Hospira Inc., Lake Forest…
  FDA Drug · Class I · 2017-05-31 · Hospira
• Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended use: For the administration of drugs and solutions to…
  FDA Device · Class II · 2017-01-18 · Hospira
• 5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 count box, Rx Only, For Spinal Anesthesia Only, Manufactured…
  FDA Drug · Class III · 2016-12-14 · Hospira
• Fentanyl Citrate Injection, USP, 100 mcg Fentanyl/ 2mL, Single Dose, 50 mcg/mL, Rx only, Hospira, Inc., Lake Forest IL 60045, NDC 0409-4093…
  FDA Drug · Class II · 2016-11-30 · Hospira
• Symbiq Two Channel Infuser
  FDA Device · Class II · 2016-11-16 · Hospira

All Hospira recalls

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0254-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.