Magic3 Go Intermittent Urinary Catheters recall: Sterility Concern
Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G
Why was Magic3 Go Intermittent Urinary Catheters recalled?
Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.
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?
a) REF 52810G, UDI/DI 00801741136870, Lot Numbers: JUGW1445
- Product
- Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G
- Recalling firm
- C.R. Bard Inc
- Quantity
- 5760 devices
- Distribution
- Worldwide
- Recall date
- June 14, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)