Remel Inc: Medical Device Recall in 2014 - (Recall #: Z-0200-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Oxoid Legionella BCYE Growth Supplement SR0110A, packaged in 100 ml vials, 10/pkg. A growth supplement for the isolation of Legionella.

Product Classification:

Class II

Date Initiated: October 17, 2014

Date Posted: November 19, 2014

Recall Number: Z-0200-2015

Event ID: 69521

Reason for Recall:

Recalled product may not provide adequate recovery of Legionella pneumophila when used as directed and may result in false negative identification of Legionella pneumophila.

Status: Terminated

Product Quantity: 16/10/100 ml, vial, pkgs

Code Information:

Lot Number: 1451506 Expiration: 26Feb2016

Distribution Pattern:

Distributed in the states of ND, VT and TX.

Voluntary or Mandated:

Voluntary: Firm initiated