Reliance Medical Products Inc: Medical Device Recall in 2018 - (Recall #: Z-1318-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical device, as part of system to store and position ophthalmological examination and diagnostic equipment, is to store and position for examination a device commonly known as a refractor.

Product Classification:

Class II

Date Initiated: December 6, 2017

Date Posted: April 18, 2018

Recall Number: Z-1318-2018

Event ID: 79601

Reason for Recall:

Product has been found with a missing Washer, Retaining Ring, and/or Stop Screw. Recalling firm was notified by distributor that Refractor Suspension Arm fell on a patient s lower torso along with the arm housing

Status: Terminated

Product Quantity: 933 ( of which 97 has been quarantined)

Code Information:

Model Number: 525004, 05 and 525006, 07

Distribution Pattern:

Worldwide Distribution - USA(nationwide) Distribution to the states of : NJ, CA, OH, VA, MA, MN, IL , UT, TN, AR, LA, AZ, PA, TX, IA and HI., and to the countries of : Costa Rica, Jamaica, South Africa, New Zealand, South Korea, Dubai, Saudi Arabia and Jordan.

Voluntary or Mandated:

Voluntary: Firm initiated