D-0713-2021 Class I Terminated
FDA drug recall D-0713-2021 was initiated by Med Shop Total Care Inc. on Oct 5, 2020 and is designated Class I. Reason for recall: Non-Sterility The recall status is terminated (terminated Aug 17, 2023). Affected quantity: 21 mL.
Recall Details
- Product Type
- Drugs
- Report Date
- Aug 18, 2021
- Initiation Date
- Oct 5, 2020
- Termination Date
- Aug 17, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 21 mL
Product Description
MORPHINE-BUPIVACAINE-KETAMINE PF INJECTABLE 21 mL syringe in two strengths: a) 5MG-25MG-5MG/ML, b) 1MG-2MG-100MCG/ML, Rx only, Med Shop Total Care 470 East Loop 281 Longview, TX 75605
Reason for Recall
Non-Sterility
Distribution Pattern
Texas and Puerto Rico
Code Information
Lot #: 09302020@31, BUD 10/28/2020, b) 09302020@29, BUD 10/30/2020
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0713-2021
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026