PlainRecalls
FDA Devices Moderate Class II Terminated

Connection Screw for NCB Plate, Item No. 0202266002

Reported: November 13, 2019 Initiated: October 10, 2019 #Z-0330-2020

Product Description

Connection Screw for NCB Plate, Item No. 0202266002

Reason for Recall

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Details

Recalling Firm
Zimmer Biomet, Inc.
Units Affected
5,459,583 total devices
Distribution
Distributed nationwide.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
Connection Screw for NCB Plate, Item No. 0202266002. Recalled by Zimmer Biomet, Inc.. Units affected: 5,459,583 total devices.
Why was this product recalled?
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Which agency issued this recall?
This recall was issued by the FDA Devices on November 13, 2019. Severity: Moderate. Recall number: Z-0330-2020.