Central Admixture Pharmacy Services, Inc.: Drug Recall

Recall #D-0949-2023 · 07/14/2023

Class II: Risk

Recall Details

Recall Number: D-0949-2023
Classification: Class II
Product Type: Drug
Recalling Firm: Central Admixture Pharmacy Services, Inc.
Status: Terminated
Date Initiated: 07/14/2023
Location: Phoenix, AZ, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 26,208 Syringes

Reason for Recall

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

Product Description

succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue Pheonix, AZ, NDC 72196-6011-2.

Distribution Pattern

Nationwide in the USA

Other Recalls by Central Admixture Pharmacy Services, Inc.

Class I: Dangerous 02/20/2025

Presence of Particulate Matter
Class II: Risk 09/21/2023

Lack of assurance of sterility:
Class II: Risk 09/21/2023

Lack of assurance of sterility:
Class II: Risk 09/21/2023

Lack of assurance of sterility:
Class II: Risk 09/21/2023

Lack of assurance of sterility:

View all recalls by Central Admixture Pharmacy Services, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.