Sterile Betadine recall: Sterility Concern
STERILE BETADINE, REF DYNDA1998
Why was Sterile Betadine recalled?
The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
UDI/DI 40889942651062 (case), 10889942651061 (each), Lot numbers: 2023042190, 2022101090, 2022081590, 2022041390, 2022031090, 2022011290, 2021100490
- Product
- STERILE BETADINE, REF DYNDA1998
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 1800 units
- Distribution
- US Nationwide distribution in the states of CT, IA, LA, MA, PA, CA, NY, FL.
- Recall date
- December 20, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)