Aaren Scientific Inc.: Medical Device Recall in 2017 - (Recall #: Z-0071-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

AERO IOL Injection System containing 10 Z28 Cartridges per box, Part #003500-0025-282, Sterile, Rx. The firm name on the label is Aaren Scientific Inc., Ontario, CA. Used to fold and insert the firm's IOL's.

Product Classification:

Class II

Date Initiated: September 1, 2017

Date Posted: November 15, 2017

Recall Number: Z-0071-2018

Event ID: 78037

Reason for Recall:

The recommended storage temperature on the label is incorrect.

Status: Terminated

Product Quantity: 786 boxes

Code Information:

Lot numbers and expiration dates: 160204, 1/31/2018; 160505, 4/30/2018; 161006, 9/30/2018; 161018, 9/30/2018; 161028, 9/30/2018; 161219, 11/30/2018; and 170120, 12/31/2018.

Distribution Pattern:

Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated