Teleflex Medical: Medical Device Recall in 2018 - (Recall #: Z-1193-2018)

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:

Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.

Product Classification:

Class II

Date Initiated: February 15, 2018

Date Posted: April 4, 2018

Recall Number: Z-1193-2018

Event ID: 79301

Reason for Recall:

Some boxes are labeled as Visistat Wide devices, when in fact the contain Visistat Regular devices. The 6 individually packaged units within the boxes are correctly labeled.

Status: Terminated

Product Quantity: 12 units

Code Information:

Lot Number 73H1600207

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated