Hill-Rom, Inc.: Medical Device Recall in 2015 - (Recall #: Z-1820-2015)

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:

Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.

Product Classification:

Class II

Date Initiated: March 2, 2015

Date Posted: July 1, 2015

Recall Number: Z-1820-2015

Event ID: 70675

Reason for Recall:

The metal cannula attached to the handpiece can rotate and become dislodged from the plastic handpiece.

Status: Terminated

Product Quantity: 66691 units

Code Information:

Product #s: 157400; 257400; 157500; 257500

Distribution Pattern:

Worldwide Distribution-US (nationwide) including the states of MI & PA, and the countries of Belgium, England, Italy, Czech Republic, Turkey, Greece, Ireland, Scotland, Spain, and Lebanon.

Voluntary or Mandated:

Voluntary: Firm initiated