This product is a single use sterile device that is recall
This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed…
Why was This product is a single use sterile device that is recalled?
Expired Products distributed to customers
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?
GTIN: 07613327118438 Lot Number: 1000388946
- Product
- This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed…
- Recalling firm
- Stryker Corporation
- Quantity
- 8 units
- Distribution
- US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.
- Recall date
- July 10, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)