Trident 10 degrees X3 Insert 36 mm ID recall
Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component
Why was Trident 10 degrees X3 Insert 36 mm ID recalled?
it was discovered that item 623-10-36I Lot 3Y0KHP, although meeting all device specifications, was determined to be unacceptable due to a documentation issue. However the parts were inadvertently shipped to the field.
What should I do if I have this product?
Review the official FDA enforcement record for current 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 3Y0KHP
- Product
- Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Quantity
- 16 units
- Distribution
- Distributed in WI.
- Recall date
- September 30, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)