Biomet Microfixation, LLC recalls Thinflap System Case The cases hold surgical instrumentation in place during handling and storage.

Recalled October 28, 2015 · FDA recall Z-0137-2016 · Biomet Microfixation

Hazard

The lids on implant caddies within P/N 17-5000 and 19-5000 could not be opened by the user without application of undesirable/unexpected excessive force. · FDA Class II

Units

5 units

Sold at

Nationwide Distribution including CA, FL, OK, NY, NC, and IL.

Description

The lids on implant caddies within P/N 17-5000 and 19-5000 could not be opened by the user without application of undesirable/unexpected excessive force.

Product

Thinflap System Case The cases hold surgical instrumentation in place during handling and storage.

Manufacturer(s)

Biomet Microfixation, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →