FDA Device Recalls

Recalls /

#136454

Product

Biomet Cobalt-Chrome Femoral Components, 32MM MOD HEAD COCR -6MM NECK; 32MM MOD HEAD COCR -3 MM NECK; 32MM MOD HEAD COCR STD NECK ; 32MM MOD HEAD COCR +3MM NECK; 32MM COCR MOD HD +6MM NO SKIRT Hip joint replacement components include: femoral stems, femoral heads, acetabular shells, and acetabular liners.

FDA product code
JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Device class
Class 2
Medical specialty
Orthopedic
510(k) numbers
K911684
Affected lot / code info
Part Numbers: 163667; 163668; 163669; 163670; 163674; Use-by 2025-03-18; Lot Numbers: 331620; 331650; 453080; 453090; 453110; 453120; 489140; 453180; 471380; 471410; 044600; 332720; 375590; 375620; 375630; 375640; 375650; 465840; 466050; 470060; 471430; 471440; 471450; 375660; 375670; 375700; 453220

Why it was recalled

Biomet hip joint, knee joint and shoulder joint replacement components device labeling contains incorrect GTIN (Global Trade Identification Number) codes.

Root cause (FDA determination)

Labeling mix-ups

Action the firm took

Biomet sent an Urgent Medical Device Recall Notice letter dated April 29, 2015 to affected customers via Fed-Ex. The letter identifed the affected product, problem and actions to be taken. Customers were asked to complete the attached response form and return it along with recalled product to Biomet. For questions callt (574) 372-1570, Monday through Friday, 8 a.m. to 5 p.m.

Recalling firm

Firm
Biomet, Inc.
Address
56 E Bell Dr, Warsaw, Indiana 46582-6989

Distribution

Distribution pattern
Worldwide Distribution - US Nationwide in the states of AR, CA, IL, IN, PA, FL, KS, LA, WI, VA, MA, MD, NJ, UT, NC, TX, AL, MI, KY, OH, SD, MO, GA, NV, WA and the countries of: Europe, Canada, Japan, Chile, Korea, Mexico, New Zealand, Trinidad/Tobago, Thailand, Argentina, Australia, and China.

Timeline

Recall initiated
2015-04-16
Posted by FDA
2015-06-11
Terminated
2016-05-16
Status

Source: openFDA Device Recall endpoint. Recall record ID #136454. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.