oxyTOCIN 20 units added to dextrose 5%/Lactated Ringer's 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6031-1.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot # 37-883206, 37-883207, 37-883210, 37-883213, 37-883216, 37-883217, 37-883217, Exp 04/30/2023; 37-884447, 37-884450, Exp 05/04/2023; 37-886269, Exp 05/11/2023; 37-887516, Exp 05/16/2023; 37-888306, 37-888308, 37-888310, 37-888311, Exp 05/21/2023; 37-890097, 37-890099, 37-890101, 37-890108, Exp 05/28/2023; 37-892636, 37-892637, 37-892639, 37-892640, Exp 06/06/2023; 37-894451, 37-894452, 37-894476, 37-894482, Exp 06/13/2023; 37-895311, 37-895312, 37-895313, Exp 06/18/2023; 37-895804, Exp 06/19/2023; 37-896607, Exp 06/21/2023
  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:

oxyTOCIN 20 units added to dextrose 5%/Lactated Ringer's 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6031-1.

Product Codes/Lot Numbers:

Lot # 37-883206, 37-883207, 37-883210, 37-883213, 37-883216, 37-883217, 37-883217, Exp 04/30/2023; 37-884447, 37-884450, Exp 05/04/2023; 37-886269, Exp 05/11/2023; 37-887516, Exp 05/16/2023; 37-888306, 37-888308, 37-888310, 37-888311, Exp 05/21/2023; 37-890097, 37-890099, 37-890101, 37-890108, Exp 05/28/2023; 37-892636, 37-892637, 37-892639, 37-892640, Exp 06/06/2023; 37-894451, 37-894452, 37-894476, 37-894482, Exp 06/13/2023; 37-895311, 37-895312, 37-895313, Exp 06/18/2023; 37-895804, Exp 06/19/2023; 37-896607, Exp 06/21/2023

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0702-2023

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