Teleflex Medical: Medical Device Recall in 2019 - (Recall #: Z-1686-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

RUSCH LASERTUBE (Rubber), Order No. : 102004-000080, REF 102004, SIZE I.D. mm 8,0

Product Classification:

Class II

Date Initiated: April 1, 2019

Date Posted: June 5, 2019

Recall Number: Z-1686-2019

Event ID: 82552

Reason for Recall:

The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

Status: Terminated

Product Quantity: 2325 units

Code Information:

Lot Numbers: 14151, 14161, 14201, 14281, 14301, 14321, 14431, 14491, 14511, 15041, 15371, 15441, 16071, 16131, 16191, 16221, 16241, 16271, 16311, 16371, 16391, 16441, 16451, 16481, 16491, 17091, 17121, 17181, 17211, 17241, 17281, 17351, 17381, 17451, 17471, 17491, 18181, 18301, 18411

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated