FDA recall record

Biomet TSP Hip Fracture Plating System device, fixation, proximal femoral, implant The recall — FDA Z-2240-2016

The screw may fracture at the junction of the shaft and the head during implantation. The patient may retain a foreign body if the fractured screw cannot…

Class IIclassification
Z-2240-2016official record ID
Jul 27, 2016report date

Recall record at a glance

Official recordZ-2240-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBiomet, Inc.
Report dateJul 27, 2016
Recall initiation dateJun 10, 2016
Quantity5458 units
LocationWarsaw, IN, United States

Official product description

TSP Hip Fracture Plating System device, fixation, proximal femoral, implant The Biomet Hip Fracture Plating Systems are indicated for use in the open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures and intertrochanteric fractures. Fracture plates with six or more femoral shaft fixation screw holes are also indicated for subtrochanteric fractures as well as proximal femoral osteotomies

Why the product was recalled

The screw may fracture at the junction of the shaft and the head during implantation. The patient may retain a foreign body if the fractured screw cannot be removed. Soft tissue irritation will not occur as the retained portion of the screw is below the surface of the plate. A delay in surgery less than 30 minutes may occur.

Distribution information

Worldwide Distribution - US (Nationwide) Internationally to Australia, The Netherlands, and Japan

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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