D-1499-2019 Class II Terminated

Recalled by Pharma-Natural Inc. — Miami Lakes, FL

FDA drug recall D-1499-2019 was initiated by Pharma-Natural Inc. on June 21, 2019 and is designated Class II. Reason for recall: CGMP Deviations: products were manufactured with lack of process validation, cleaning validation, stability studies, and other current good manufacturing practice violations. The recall status is terminated (terminated October 27, 2021). Affected quantity: 2000 roll on bottles.

Recall Details

Product Type
Drugs
Report Date
July 31, 2019
Initiation Date
June 21, 2019
Termination Date
October 27, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2000 roll on bottles

Product Description

LidoAID (Lidocaine HCL 4%) portable pain relieving TOPICAL ANALGESIC GEL, 0.17 Oz (4 g) roll on bottle, Distributed by: Diabetic Supply of Suncoast, Inc., dba Advocate Diabetes, PO Box 2102, Vega Alta, PR 00692, NDC 63788-114-04.

Reason for Recall

CGMP Deviations: products were manufactured with lack of process validation, cleaning validation, stability studies, and other current good manufacturing practice violations.

Distribution Pattern

Consignees in FL and TX who may have further distributed Nationwide in the USA and Puerto Rico.

Code Information

All lots remaining within expiry.