Command Instrument Broach Handle. Used in Total Hip recall
Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog Number: 6266-0-100
Why was Command Instrument Broach Handle. Used in Total Hip recalled?
Reports of handle fracture and subsequent disassociation of cam assembly subcomponents during use.
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: 6266-0-100 Lot Code: RD6W017, RD7L234X, RD7L234, RD7L235, RD5T305A, RD6W017J, RD6W017A, RD5T307, RD5T305T, RD5T305M, RD5T305L, RD5T306X, RD5T305, RD5T306
- Product
- Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog Number: 6266-0-100
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Quantity
- 48 units
- Distribution
- Nationwide Distribution.
- Recall date
- March 20, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)