PlainRecalls
FDA Devices Moderate Class II Terminated

CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201 00223200202

Reported: November 13, 2019 Initiated: October 10, 2019 #Z-0327-2020

Product Description

CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201 00223200202

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?
CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201 00223200202. 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-0327-2020.