FDAClass IISeptember 21, 2022

L-Carnitine 500 mg/mL Injectable recall: Sterility Concern

L-Carnitine 500 mg/mL Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.

Why was L-Carnitine 500 mg/mL 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?

Lot: 06132022@17; BUD: 02/15/2023

Product
L-Carnitine 500 mg/mL Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.
Recalling firm
Carolina Infusion
Quantity
1 vial
Distribution
Nationwide in the USA.
Recall date
September 21, 2022
Classification
Class II
Status
Completed
Agency
FDA (drug)
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