Stryker Orthopaedics Navigation Compatible Accolade recall
Stryker Orthopaedics Navigation Compatible Accolade Broach Handle 1 single unit to a package Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ…
Why was Stryker Orthopaedics Navigation Compatible Accolade recalled?
Stryker received reports from the field of the impaction plate dissociating/fracturing from the main body of the broach handle.
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?
Catalog no. 2124-1400 All lots
- Product
- Stryker Orthopaedics Navigation Compatible Accolade Broach Handle 1 single unit to a package Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ…
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Quantity
- 211 units
- Distribution
- IL MA, MN, ND, OR, & PA
- Recall date
- February 19, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)