Insight Instruments, Inc.: Medical Device Recall in 2013 - (Recall #: Z-1281-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Insight Instruments MIS ( Multi-Port Illumination System) Illuminated pilot tubes work like a ceiling light while simultaneously protecting the entry sites. Illumination automatically follows the movement of the two surgical instruments inserted into the M.I.S. cannulas. The large distance of more than 16mm between cannula ends and posterior pole guarantees sufficient light in the working area and a large observation field especially when used in conjunction with modern wide field panoramic observation systems.

Product Classification:

Class II

Date Initiated: March 15, 2013

Date Posted: May 22, 2013

Recall Number: Z-1281-2013

Event ID: 64887

Reason for Recall:

Insight Instruments, Inc., Stuart, FL is recalling M.I.S. (Multi-Port Illumination System), Ophthalmic Cannula due to a misclassification of the medical device.

Status: Terminated

Product Quantity: 776

Code Information:

Lot Numbers: M53157, M55115, M56929, M58551, M61862.

Distribution Pattern:

US Distribution IN and IL

Voluntary or Mandated:

Voluntary: Firm initiated