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Various trauma and sports medicine instruments and implants recallZ-1823-2016 · Biomet, Inc. · initiated Apr 1, 2016

Class II Terminated All recalls posted in May 2016

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Biomet, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Insufficient seal strength on sterile barrier packaging. The seal could be jeopardized causing the sterile barrier to be compromised and the product could become nonsterile. If the product becomes non-sterile and is used or implanted, it may lead to an infection.

FDA root cause category: Equipment maintenance

What the company is doing

Zimmer Biomet sent an Urgent Medical Device Recall Notice dated April 1, 2016, to all affected customers. Customers were instructed to locate and return the affected product, and implanting surgeons were instructed to monitor patients. The recall notification included a description of the reason for the recall, affected product, consignee responsibilities, and instructions for responding to the formal recall notification. Questions related to this notice should be directed to (574) 372-1570, Monday through Friday, 8 a.m. to 5 p.m.

Recall details

Recall number
Z-1823-2016
Recall class
Class II
Status
Terminated
Initiated by the company
Apr 1, 2016
Posted by the FDA
May 26, 2016
Recalling firm
Biomet, Inc.
Product code
HWC
FDA submissions
K992367
Distribution
Worldwide Distribution - US (Nationwide) and globally to Argentina, Australia, Brazil, Canada, Chile, Colombia, Costa Rica, Ecaudor, The Netherlands, Japan, Korea, Malaysia, Mexico, Peru.

Product description

Various trauma and sports medicine instruments and implants. Screw, fixation, bone.

Code information (models, lots, serial numbers)

Part #'s HAA60-11030 HAA60-13030 HAA60-15040 HAA60-16040 HAA60-18040  Lot #'s 016150 016210 165130 016230 133890 181600 133970 134000 181620

Other devices under the same FDA submission

64 devices cleared under K992367 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.

Other products in the same recall event

The FDA groups related products into one recall event (event 74038).

Sources and updates

How recalls are matched to devices · Editorial policy · Report an error on this page