TRI-MIX 30/1/40 Injectable recall: Sterility Concern
TRI-MIX 30/1/40 Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.
Why was TRI-MIX 30/1/40 Injectable recalled?
Lack of Assurance of Sterility
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lots: 07052022@8, BUD: 09/03/2022; 07292022@10, BUD: 09/27/2022
- Product
- TRI-MIX 30/1/40 Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.
- Recalling firm
- Carolina Infusion
- Quantity
- 2 vials
- Distribution
- Nationwide in the USA.
- Recall date
- September 21, 2022
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (drug)