Amerisource Health Services LLC: Drug Recall

Recall Details

Recall Number

D-0368-2025

Classification

Class II

Product Type

Drug

Recalling Firm

Amerisource Health Services LLC

Status

Ongoing

Date Initiated

04/02/2025

Location

Columbus, OH, United States

Voluntary/Mandated

Voluntary: Firm initiated

Product Quantity

14,189 vials

Reason for Recall

Lack of assurance of sterility. Bacterial contamination detected in some media fill units

Product Description

Haloperidol Decanoate Injection, 100 mg/mL*, 1 x 1 mL Single-Dose Vial, Rx only, Manufactured by: Somerset Therapeutics Limited, #54/1, Boodhihal Village, Nelamangala, Bangalore - 562123, Karnataka, India, Manufactured for BluePoint Laboratories, NDC 68001-581-41.

Distribution Pattern

Nationwide in the USA

Other Recalls by Amerisource Health Services LLC

• Class II: Risk 10/16/2025
  Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit
• Class II: Risk 10/16/2025
  Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit
• Class II: Risk 10/16/2025
  Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit
• Class II: Risk 10/09/2025
  CGMP Deviations: The recalling firm filed for Chapter 11 on September 30, 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.
• Class II: Risk 09/15/2025
  Failed Dissolution Specifications.

View all recalls by Amerisource Health Services LLC →