Catalog A800061 recall: Sterility Concern
Catalog A800061, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
Why was Catalog A800061 recalled?
There is potential for packaging defects that may impact the sterile barrier.
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?
Catalog A800061, Lot NGFR3658, UDI (01)00801741104848(17)251228(10)
- Product
- Catalog A800061, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
- Recalling firm
- C.R. Bard Inc
- Quantity
- 2660 units
- Distribution
- US Nationwide distribution.
- Recall date
- September 29, 2021
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)