Ziemer Usa Inc: Medical Device Recall in 2015 - (Recall #: Z-0988-2015)

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:

Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries.

Product Classification:

Class II

Date Initiated: December 18, 2014

Date Posted: January 21, 2015

Recall Number: Z-0988-2015

Event ID: 70024

Reason for Recall:

The devices were not shipped with the Starter Kits.

Status: Terminated

Product Quantity: 26 lasers

Code Information:

Serial Numbers: FLM4184, FLM2003, FLM3324, FLM1409, FLM2906, FLM2136, FLM4948, FLM3134, FLM4587, FLM3281, FLM2179, FLM1467, FLM1239, FLM3361, FLM3319, FLM3685, FLM2915, FLM1230, FLM3229, FLM4094, FLM4135, FLM4545, FLM4905, FLM3913, FLM1680, FLM1776

Distribution Pattern:

US: Nationwide (AL, CA, FL, GA, IL, MN, MO, NC, ND, NH, NJ, NM, NY, PA, TX, VA, WA)

Voluntary or Mandated:

Voluntary: Firm initiated