Home / Recalls / Medical Devices
Remel Inc recalls Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood
Recalled May 3, 2017 · FDA recall Z-1888-2017 · Remel
Hazard
Confirmed complaint of surface contamination of Listeria monocytogenes. · FDA Class II
Units
1,159/100 plates/packs
Sold at
US Nationwide distribution in the states of : AR, AZ, CO, IA, IL, KS, KY, LA, MI, MO, MS, MT, NC, ND, NE, NM, OH, OK, SD, and TX and Puerto Rico
Description
Confirmed complaint of surface contamination of Listeria monocytogenes.
Product
Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: 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.
Manufacturer(s)
Remel Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →