FDAClass IIAugust 27, 2025

Brand Name: Q-Stop Product Name: Suture Retention recall

Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog Number: QS Software Version: N/A Product Description: The DRS Vascular Q-Stop…

Why was Brand Name: Q-Stop Product Name: Suture Retention recalled?

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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?

Lot Code: 00860011629405 (6-pack) Unit of use: 10860011629402

Product
Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog Number: QS Software Version: N/A Product Description: The DRS Vascular Q-Stop…
Recalling firm
Drs Vascular, Inc
Quantity
264
Distribution
U.S. Nationwide distribution in the states of AR, CA, and NY.
Recall date
August 27, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls