Noven Therapeutics, LLC: 7 recalls on record

Recalls filed with 1 agency: FDA (7).

First recall on record: March 25, 2020. Most recent: April 29, 2020.

Risk classification: Class II: 7

Most recent recalls

DateAgencyProduct
April 29, 2020FDADaytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr), 30…D-1247-2020
April 29, 2020FDADaytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours (3.3 mg/hr) 30-…D-1249-2020
April 29, 2020FDADaytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours (2.2 mg/hr) 30-…D-1248-2020
March 25, 2020FDADaytrana (methylphenidate transdermal system) patches, Delivers 20 mg over 9 hours (2.2 m…D-1044-2020
March 25, 2020FDADaytrana (methylphenidate transdermal system) patches, Delivers 15 mg over 9 hours (1.6 m…D-1043-2020
March 25, 2020FDADaytrana (methylphenidate transdermal system) patches, Delivers 30 mg over 9 hours (3.3 m…D-1045-2020
March 25, 2020FDADaytrana (methylphenidate transdermal system) patches, Delivers 10 mg over 9 hours (1.1 m…D-1042-2020

Questions about this company

How many recalls does Noven Therapeutics, LLC have?
Recalert has 7 U.S. recalls on record for Noven Therapeutics, LLC, published between March 25, 2020 and April 29, 2020.
What was the most recent Noven Therapeutics, LLC recall?
FDA recall D-1247-2020, published April 29, 2020: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr), 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC Miami, FL 33186, NDC 68968-5552-3
Which agencies have handled Noven Therapeutics, LLC recalls?
Noven Therapeutics, LLC appears as the recalling firm in recalls from: FDA (7).

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