G & W Laboratories, Inc.: 6 recalls on record

Recalls filed with 1 agency: FDA (6).

First recall on record: January 8, 2014. Most recent: February 14, 2018.

Risk classification: Class II: 1 · Class III: 5

Most recent recalls

DateAgencyProduct
February 14, 2018FDACiclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15); b) 30 …D-0250-2018
July 12, 2017FDAG & W Clobetasol Propionate Ointment 0.05%, packaged in a) 15 g tube (NDC 0713-0656-15), …D-0945-2017
April 12, 2017FDACiclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15), b) 30 …D-0636-2017
March 22, 2017FDAClindamycin Phosphate Topical Solution USP, 1%, packaged in a) 30 mL applicator bottles (…D-0519-2017
March 8, 2017FDAIndocin (Indomethacin) suppositories, USP, 50 mg, laminate strips packed in boxes of 30, …D-0501-2017
January 8, 2014FDAG & W Fluocinolone Acetonide Cream USP 0.025%, a) 15 gm (NDC 0713-0222-15), b) 60 gm (NDC…D-391-2014

Questions about this company

How many recalls does G & W Laboratories, Inc. have?
Recalert has 6 U.S. recalls on record for G & W Laboratories, Inc., published between January 8, 2014 and February 14, 2018.
What was the most recent G & W Laboratories, Inc. recall?
FDA recall D-0250-2018, published February 14, 2018: Ciclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15); b) 30 g tubes (NDC 0713-0638-31); and c) 90 g tubes (NDC 0713-0638-18), Rx Only, Manufactured by: G&W Laboratories, …
Which agencies have handled G & W Laboratories, Inc. recalls?
G & W Laboratories, Inc. appears as the recalling firm in recalls from: FDA (6).

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