Remel Inc: Medical Device Recall in 2014 - (Recall #: Z-0578-2015)

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 packaged in packs of 10-100ml vials. A growth supplement for the isolation of Legionella.

Product Classification:

Class II

Date Initiated: November 13, 2014

Date Posted: December 17, 2014

Recall Number: Z-0578-2015

Event ID: 69771

Reason for Recall:

Use of the product could result in inadequate recovery of Legionella pneumophila which could result in false negative reporting.

Status: Terminated

Product Quantity: 1/10/100 ml/vials/packs

Code Information:

Lot number: 1374439, Exp: 31 Aug 2015

Distribution Pattern:

Nationwide Distribution to FL

Voluntary or Mandated:

Voluntary: Firm initiated