Bard Clean-Cath Intermittent Catheter recall
Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological use only.
Why was Bard Clean-Cath Intermittent Catheter recalled?
The device catheter tip was cut off (no tip) and the product packaging was not fully sealed.
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?
Cat. No. 420712/Lot No. NGDY1813/ UDI (GTIN) (01)00801741038730(17)241130(10), Exp. Date 11/30/2024
- Product
- Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological use only.
- Recalling firm
- C.R. Bard, Inc.
- Quantity
- 9,800 Units
- Distribution
- Worldwide distribution - US Nationwide distribution and the countries of Australia, Canada.
- Recall date
- April 28, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)