FDAClass IIOctober 2, 2024

Biodesign Recto-Vaginal Fistula Plug RVP-0.2 - For recall: Labeling Error

Biodesign Recto-Vaginal Fistula Plug RVP-0.2 - For implantation to reinforce soft tissue for repair of recto-vaginal fistulas. Order Number (GPN)…

Why was Biodesign Recto-Vaginal Fistula Plug RVP-0.2 - For recalled?

Products expire prior to the expiration date printed on the product labeling

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: (01)00827002466012(17)250603(10)LB1534431 Lot Number: LB1534431

Product
Biodesign Recto-Vaginal Fistula Plug RVP-0.2 - For implantation to reinforce soft tissue for repair of recto-vaginal fistulas. Order Number (GPN)…
Recalling firm
Cook Biotech, Inc.
Quantity
3 units
Distribution
Worldwide distribution - US Nationwide and the countries of Australia, Austria, Canada, China, Finland, France, Germany, Ireland, Luxembourg, Netherlands, New Zealand, Norway, South Africa, United Kingdom.
Recall date
October 2, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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