LL-37 2 mg/mL (5 mL) Injection, 5 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson,...

FDA Recall #D-0778-2022 — Class II — April 5, 2022

Recall #D-0778-2022 Date: April 5, 2022 Classification: Class II Status: Terminated

Product Description

LL-37 2 mg/mL (5 mL) Injection, 5 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA

Reason for Recall

Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.

Recalling Firm

North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding — Richardson, TX

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

25 vials

Distribution

Nationwide within United States

Code Information

Lot #: 33444 BUD: 4/26/2022

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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