Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral recall
Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis component.
Why was Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral recalled?
Complaints that the femoral head could not be assembled with its corresponding V40 stem trunnion at the time of surgery.
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 Numbers 6260-5-028; 6260-5-032; 6260-5-132; 6260-5-232, 232; 6260-5-328; 6260-5-332; 6260-5-428; 6260-5-432; 6260-9-0928; 6260-9-032, 6260-9-132, 6260-9-232, 6260-9-328, 6260-9-332, 6260-9-428, 6280-0-128, 6280-0-228, 6280-0-232, 6280-0-332 exp- dates july 2019 to august 2019
- Product
- Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis component.
- Recalling firm
- Stryker Howmedica Osteonics Corp.
- Quantity
- 201
- Distribution
- Nationwide Distribution
- Recall date
- November 18, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)