Skip to content
Recall Observatory FDA recall evidence

Device product

Hip Products Item Number: 1) 110010462 RingLoc Hip System, Acetabular Bi-Polar Cup, 28 MM X 51 MM 2) 11-165218 RingLoc Bi-Polar Hip System, Acetabular Cup, 28 MM X 47 MM 3) XL-105916 588500 RingLoc Hip System, Acetabular Liner, 36 MM, Size 26 Product Usage: Hemi hip arthroplasty.

Z-2145-2020

April 17, 2020

Class II

Product summary

Firm
Biomet, Inc.
Event
Event 85524
Status
Terminated
Classification
Class II
Quantity
58 units
Official record key
device-enforcement:Z-2145-2020

Official wording

Reason: Potential presence of elevated endotoxin levels that exceed the specification limit

Code information: Lot Numbers: UDI Number 1) 752470 (01)00880304568785(17)220118(10)752470 854070 (01)00880304568785(17)220119(10)854070; 2) 094360 (01)00880304209688(17)220106(10)094360; 3) 588500 (01)00880304209688(17)220106(10)094360

Distribution pattern: Worldwide distribution - US Nationwide distribution and the countries of Canada, AHMADABAD, GUJARAT, BANGKOK, BELROSE NSW, BUENOS AIRES, CHILE, COSTA RICA, HIRATSUKA CITY, HUECHURABA SANTIAGO, INDIA, JAPAN, MEXICO DF, NETHERLANDS, PICHINCHA, EC, SAN JOSE, SINGAPORE, TAIWAN, THAILAND, YONGSAN-GU SEOUL.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potential presence of elevated endotoxin levels that exceed the specification limit