U.S. FOOD AND DRUG ADMINISTRATION: Biomet RingLoc Hip System SelfTapping Bone Screw


U.S. Food and Drug Administration recently issued the following announcement.

Date Initiated by Firm: March 01, 2019

Create Date: April 04, 2019

Recall Status: Open, Classified

Recall Number: Z-1086-2019

Recall Event ID: 82332

510(K)Number: K912245  

Product Classification: Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer - Product Code JWH

Product: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile Titanium. Accessory to total hip implant

Item Number: 103531

Product Usage: Accessory to total hip implant

Code Information: Lot Numbers/UDI Number 523430 (01) 00880304001961 (17) 280804 (10) 523430 523450 (01) 00880304001961 (17) 280727 (10) 523450 860840 (01) 00880304001961 (17) 280806 (10) 860840 860850 (01) 00880304001961 (17) 280809 (10) 860850 860860 (01) 00880304001961 (17) 280806 (10) 860860

Recalling Firm/Manufacturer: Zimmer Biomet, Inc.

                                                   56 E Bell Dr

                                                   Warsaw IN 46582-6989

For Additional Information Contact: 411 Technical Services

                                                          574-371-3071

Manufacturer Reason

Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have the potential for the 30mm screws to be packaged as 20mm screws and vice versa.

FDA Determined Cause: Packaging process control

Action: Zimmer Biomet conducted recall by letter dated 3/1/19 to the consumer/user level, including any intermediate wholesale or retail consignees. All distributors via email. Hospital risk managers and surgeons, as well as distributors with product notified Fed'x. Accounts asked to review notification and ensure that affected team members are aware of the contents. 2. Immediately locate and quarantine affected product in your inventory.3. Immediately return all affected product from your distributorship and from affected hospitals within your territory.a. Complete Attachment 1  Inventory Return Certification Form. Questions or concerns after reviewing this notice, please call customer service at 574-371-3071 between 8:00 am and 5:00pm EST, Monday through Friday.

Quantity in Commerce: 809 total

Distribution: Worldwide Distribution - US Nationwide

Foreign:

CHILE

CHINA

COSTA RICA

GUJRAT,INDIA

JAPAN

MEXICO CDMX

SINGAPORE

Total Product Life Cycle: TPLC Device Report

Original source can be found here. 

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