SALTER LABS: Medical Device Recall in 2012 - (Recall #: Z-1898-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7 ft, oxygen tube, 7 ft. CO2 tube RX only.For Single Patient Use only. Distributed by Tri-Anium Assembled in Mexico. Usage: Delivery of Anesthesia.

Product Classification:

Class II

Date Initiated: May 30, 2012

Date Posted: July 4, 2012

Recall Number: Z-1898-2012

Event ID: 62272

Reason for Recall:

A complaint was received, and later verified, that product labeled as SO-1296 with male luer lock connector actually contained product with a female luer lock connector.

Status: Terminated

Product Quantity: 242 cases

Code Information:

Salter Part Number SO-1296, Tri-Anium Part numaber: 301-P3600; Lot number: 032612.

Distribution Pattern:

Nationwide distribution: USA including states of: FL, IN, KS, PA and TX.

Voluntary or Mandated:

Voluntary: Firm initiated