RecallHawk
Class II Recall

Fluticasone Propionate Nasal Spray USP, 50 mcg per spray, 120 metered sprays, 16 g net fill, Rx only, Manufactured by: A

Golden State Medical Supply Inc.

Summary

The FDA issued a Class II for Fluticasone Propionate Nasal Spray USP, 50 mcg per spray, 120 metered sprays, 16 by Golden State Medical Supply Inc.. Reason: CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex.

Details

Source

Drug Recall

External ID

D-0349-2024

Action Date

2024-03-06

Status

Ongoing

Category

drug

Product Description

Fluticasone Propionate Nasal Spray USP, 50 mcg per spray, 120 metered sprays, 16 g net fill, Rx only, Manufactured by: Apotek Inc., Toronto, Ontario, Cananda, Marketed by: GSMS Incorporated, Camarillo, CA, NDC 60429-195-15

Lot/Code Info: Lot #: TX5275, Exp. Date: 10/31/2026.

Quantity Affected: 59,712 bottles

Reason for Recall

CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex

Distribution

Nationwide in the USA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-02-14

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 63 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

Golden State Medical Supply Inc. has 23 FDA actions in our database, including 23 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 (Golden State Medical Supply Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Golden State Medical Supply Inc. have FDA actions?

Golden State Medical Supply Inc. has 23 FDA actions in our database, including 23 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0349-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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