Remel Inc: Medical Device Recall in 2015 - (Recall #: Z-1748-2015)

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:

Remel Blood Agar (TSA w/sheep blood) plate REF R01202 packaged 10 plates per pack, 10/10-packs per case (100 plates). Blood agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic reactions.

Product Classification:

Class II

Date Initiated: May 4, 2015

Date Posted: June 17, 2015

Recall Number: Z-1748-2015

Event ID: 71198

Reason for Recall:

Product may be contaminated with Listeria monocytogenes.

Status: Terminated

Product Quantity: 845/10/10-plate pack cases

Code Information:

Lot Number: 646595 and 646596 Expiration date: 19May2015

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated