Biomet Microfixation, LLC: Medical Device Recall in 2015 - (Recall #: Z-0137-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 6, 2015

Date Posted: October 28, 2015

Recall Number: Z-0137-2016

Event ID: 72366

Reason for Recall:

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.

Status: Terminated

Product Quantity: 5 units

Code Information:

Lot Code # 101465 Model # 19-5000

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated