LL-37 2 mg/mL (5 mL) Injection, 5 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA
North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding
Summary
The FDA issued a Class II for LL-37 2 mg/mL (5 mL) Injection, 5 mL vials, Rx only, Farmakeio 1736 N Greenvill by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding. Reason: Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended.
Details
Source
Drug Recall
External ID
D-0778-2022
Action Date
2022-04-27
Status
Terminated
Category
drug
Product Description
LL-37 2 mg/mL (5 mL) Injection, 5 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA
Lot/Code Info: Lot #: 33444 BUD: 4/26/2022
Quantity Affected: 25 vials
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.
Distribution
Nationwide within United States
Type: Voluntary: Firm initiated
Recall Initiated: 2022-04-05
Company
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 31 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding has 7 FDA actions in our database, including 7 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding have FDA actions?
North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0778-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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