vancomycin added to dextrose 5%, 1.5 g/250 mL* (6 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6075-1.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot # 37-883196, 37-883197, 37-883205, Exp 04/30/2023; 37-884882, 37-884890, 37-884898, Exp 05/07/2023; 37-886840, 37-886858, 37-886863, Exp 05/15/2023; 37-887365, Exp 05/16/2023; 37-887663, Exp 05/17/2023; 37-888254, 37-888257, 37-888265, 37-888303, Exp 05/21/2023; 37-889453, Exp 05/24/2023; 37-890037, 37-890039, 37-890043, Exp 05/28/2023; 37-890330, 37-890333, 37-890344, Exp 05/29/2023; 37-892009, 37-892011, 37-892016, Exp 06/05/2023; 37-892881, Exp 06/07/2023; 37-893448, Exp 06/11/2023; 37-895221, Exp 06/18/2023; 37-898530, Exp 06/29/2023
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Central Admixture Pharmacy Services, Inc.
Reason for Recall:
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

vancomycin added to dextrose 5%, 1.5 g/250 mL* (6 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6075-1.

Product Codes/Lot Numbers:

Lot # 37-883196, 37-883197, 37-883205, Exp 04/30/2023; 37-884882, 37-884890, 37-884898, Exp 05/07/2023; 37-886840, 37-886858, 37-886863, Exp 05/15/2023; 37-887365, Exp 05/16/2023; 37-887663, Exp 05/17/2023; 37-888254, 37-888257, 37-888265, 37-888303, Exp 05/21/2023; 37-889453, Exp 05/24/2023; 37-890037, 37-890039, 37-890043, Exp 05/28/2023; 37-890330, 37-890333, 37-890344, Exp 05/29/2023; 37-892009, 37-892011, 37-892016, Exp 06/05/2023; 37-892881, Exp 06/07/2023; 37-893448, Exp 06/11/2023; 37-895221, Exp 06/18/2023; 37-898530, Exp 06/29/2023

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0721-2023

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