Stryker Orthopaedics Ball Impactor Tip Product Usage recall
Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM Surgery.
Why was Stryker Orthopaedics Ball Impactor Tip Product Usage recalled?
Stryker has received complaints associated with cracks and/or fracture of the Ball Impactor Tip and Rim Impactor Tip Instruments.
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 number 1235-0-014 all lot codes
- Product
- Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM Surgery.
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Quantity
- 1,024 units
- Distribution
- USA Nationwide Distribution
- Recall date
- January 1, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)