PlainRecalls
FDA Devices Moderate Class II Terminated

RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item XL-108323 ArComXL MaxRom +3mm Liners Size 23 item XL-108223

Reported: January 25, 2017 Initiated: December 19, 2016 #Z-1024-2017

Product Description

RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item XL-108323 ArComXL MaxRom +3mm Liners Size 23 item XL-108223

Reason for Recall

Product complaints indicated that the part and lot numbers on the packaging differed from the physical product inside the packaging. Risk of delay in surgery.

Details

Recalling Firm
Zimmer Biomet, Inc.
Units Affected
36
Distribution
USA (nationwide) and Internationally to ARGENTINA
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item XL-108323 ArComXL MaxRom +3mm Liners Size 23 item XL-108223. Recalled by Zimmer Biomet, Inc.. Units affected: 36.
Why was this product recalled?
Product complaints indicated that the part and lot numbers on the packaging differed from the physical product inside the packaging. Risk of delay in surgery.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 25, 2017. Severity: Moderate. Recall number: Z-1024-2017.