US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 16, 2018 (8 years ago)

fas.TRACT Coagulative Hemostatic Gel

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

cGMP violations noted during the firm's most recent inspection.

What was recalled

fas.TRACT Coagulative Hemostatic Gel, 10% Ferric Sulfate Kit, Rx Only, (3) 3cc Preloaded Syringes/ (50) Scrub Tips. Distributed by: Benco Dental, 295 Center Point Blvd., Pittston, PA 18640. NDC: 14060-01105

Recalling firm
CAO Group, Inc.
Origin
UT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0290-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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Class III · Low risk Ongoing

Premier

Reason Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that this error is limited to the vial itself; the saleable unit of the box of 12 bottles has the correct expiration date printed.

Premier Dental Products Co NDC 48783-112-08 D-0490-2026
Class II · Moderate risk Completed

AstrinGyn

Reason CGMP Deviations: Products not manufactured under current good manufacturing practices.

Ecometics, Inc. NDC 59365-6065-0 D-1101-2023
Class II · Moderate risk Terminated

Auryxia

Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Cardinal Health Inc. NDC 59922-631-01 D-0499-2021
Class III · Low risk Terminated

Auryxia

Reason Failed Dissolution Specifications

Akebia Therapeutics dba Keryx Biopharmaceutials, Inc NDC 59922-0631-01 D-0260-2021
Class II · Moderate risk Terminated

Auryxia

Reason CGMP Deviations

Akebia Therapeutics dba Keryx Biopharmaceutials, Inc NDC 59922-631-01 D-0170-2021