Edta Disodium 15% recall: Sterility Concern
EDTA DISODIUM 15% (150MG/ML), 20ML Vials, MEDAUS PHARMACY
Why was Edta Disodium 15% recalled?
Lack of Assurance of Sterility
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 151202-45, BUD: 05/30/16; Lot #: 160105-38, BUD: 07/03/16; Lot #: 160114-20, BUD: 07/12/16; Lot #: 160217-28, BUD: 08/15/16
- Product
- EDTA DISODIUM 15% (150MG/ML), 20ML Vials, MEDAUS PHARMACY
- Recalling firm
- Medaus, Inc.
- Quantity
- 24000 mL in Vials
- Distribution
- U.S. Nationwide, Japan, and New Zealand.
- Recall date
- July 20, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)