Halyard VA LUMBAR LAMINECTOMY - Medical convenience recall: Foreign Material
Halyard VA LUMBAR LAMINECTOMY - Medical convenience kits Model Number: VMED009-03
Why was Halyard VA LUMBAR LAMINECTOMY - Medical convenience recalled?
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
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: 10809160393918 Lot Number: 1603129, 1605478
- Product
- Halyard VA LUMBAR LAMINECTOMY - Medical convenience kits Model Number: VMED009-03
- Recalling firm
- AVID Medical, Inc.
- Quantity
- 24 eaches
- Distribution
- US Nationwide distribution.
- Recall date
- November 20, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)