Zimmer Manufacturing B.V.: Medical Device Recall in 2016 - (Recall #: Z-1680-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 45 mm Length 47115504507 Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 75 mm Length 47115507507 Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 90 mm Length 47115509007

Product Classification:

Class II

Date Initiated: May 4, 2016

Date Posted: May 25, 2016

Recall Number: Z-1680-2016

Event ID: 73981

Reason for Recall:

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Status: Terminated

Product Quantity: 90

Code Information:

LOTS: 63303808 63292589 63292588

Distribution Pattern:

Worldwide distribution. US nationwide, Korea, Japan, Argentina, Brazil, Singapore, Taiwan, China, El Salvador, Australia, India, Hong Kong, Chile, Germany, Italy, France, Spain, UK, Sweden, Canada.

Voluntary or Mandated:

Voluntary: Firm initiated