Zimmer Biomet, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1220-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

1.5mm System, Cranio-maxillofacial Bone Screws 1.5 x 4mm HT SD X-DR Screw, Bone Screw

Product Classification:

Class II

Date Initiated: January 10, 2017

Date Posted: February 22, 2017

Recall Number: Z-1220-2017

Event ID: 76375

Reason for Recall:

The identification of the devices was non-conforming with off-centered slots and the no-go gage starting in the pilot hole.

Status: Terminated

Product Quantity: 11

Code Information:

95-6104- Item No. 530430- Lot 1.5x4mm HT SD X-DR Screw

Distribution Pattern:

Domestic: None VA/DOD: None Foreign: Japan

Voluntary or Mandated:

Voluntary: Firm initiated