Remel Inc: Medical Device Recall in 2015 - (Recall #: Z-1232-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England and Oxoid Ltd., Basingstoke, Hants, England.

Product Classification:

Class II

Date Initiated: February 5, 2015

Date Posted: March 11, 2015

Recall Number: Z-1232-2015

Event ID: 70471

Reason for Recall:

Use of the product may not provide adequate recovery and could result in false negative identification of Legionella pneumophila.

Status: Terminated

Product Quantity: 24 packs (10 x 100 ml vials)

Code Information:

Lot No. 1545171

Distribution Pattern:

US Distribution to the states of : MI, ND, SC, TN, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated