Remel Inc: Medical Device Recall in 2013 - (Recall #: Z-0801-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

The product is a lyophilized growth supplement for use with dehydrated culture media to prepare BCYE Medium used for isolation of Legionellae from clinical and environmental samples.

Product Classification:

Class II

Date Initiated: October 10, 2012

Date Posted: February 20, 2013

Recall Number: Z-0801-2013

Event ID: 63584

Reason for Recall:

The product may contain low level microbial contamination which could result in incorrect results.

Status: Terminated

Product Quantity: 10 units

Code Information:

Lot 1175209

Distribution Pattern:

Distribution included the states of IL, IN and MI.

Voluntary or Mandated:

Voluntary: Firm initiated