D-0851-2022 Class II Ongoing

Recalled by McKesson Corporation Dba McKesson Drug Company — Memphis, TN

FDA drug recall D-0851-2022 was initiated by McKesson Corporation Dba McKesson Drug Company on Apr 21, 2022 and is designated Class II. Reason for recall: CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program. The recall status is ongoing. Affected quantity: 5,640 tubes.

Recall Details

Product Type
Drugs
Report Date
May 11, 2022
Initiation Date
Apr 21, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
5,640 tubes

Product Description

Erythromycin Topical Gel USP, 2%, Net Wt 60 g tube, Rx only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310 Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-053-68

Reason for Recall

CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.

Distribution Pattern

Nationwide in the United States including Guam and the Northern Mariana Islands.

Code Information

Lot: 15723, Exp.: 06/30/2022

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-0851-2022
openFDA file date
Nov 10, 2026
Loaded by RegDataLab
Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for D-0851-2022. Report a data issue: hello@regdatalab.com.