Remel recalls

Remel has 86 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 8 Jul 2026. 17 are still ongoing. 4 were reported in the last 12 months.

Total recalls86since 2013
Last 12 months4reported
Class I910% of total
Ongoing17latest 8 Jul 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 9 10%Class II 74 86%Class III 3 3%

By year

Ongoing remel recalls

17 active

All remel recalls, newest first

86 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIGC Agar Base R04030 recalled by RemelRemelOtherNationwide
DeviceCLASS IIYeastone Broth, 10/BOX YY3462 recalled by RemelRemelOtherNationwide
DeviceCLASS IICampy CVA Medium, R01272 recalled by RemelRemelOther Bacterial ContaminationNationwide
DeviceCLASS IICamhb W/lhb, Manual, 10/box Ycp112-10 Brucella Broth, 10/box Yt3450 recalledRemelOtherNationwide
DeviceCLASS IIBlood/EMB, Levine, Product Number R02041 recalled by RemelRemelListeriaNationwide
DeviceCLASS IIStrep Selective II Agar, Product Number R01859 recalled by RemelRemelListeriaNationwide
DeviceCLASS IIBlood/MacConkey Biplate, Product Number R02049 recalled by RemelRemelListeriaNationwide
DeviceCLASS IIBlood Agar,5% Sheep Blood, Product Number R01202 recalled by RemelRemelListeriaNationwide
DeviceCLASS IIThermo Scientific Sensititre Cation Adjusted AutoRead recalled by RemelRemelOtherNationwide
DeviceCLASS IIZebra Thermal Barcode Printer GX430t recalled by RemelRemelOther17 states
DeviceCLASS IIBlood Agar MacCONKEY Agar Biplate recalled by RemelRemelListeriaNationwide
DeviceCLASS IIBlood Agar Emb Agar Biplate recalled by RemelRemelListeriaNationwide
DeviceCLASS IIBactiDrop Acridine Orange recalled by RemelRemelPackaging Defects8 states
DeviceCLASS IITodd Hewitt W recalled by RemelRemelOtherNationwide
DeviceCLASS IIHaemophilus Test Medium (Agar) recalled by RemelRemelDevice MalfunctionNationwide
DeviceCLASS IThermo Scientific Sensititre Plate, GN4F, Gram Negative IVD AST recalledRemelOtherNationwide
DeviceCLASS IThermo Scientific, Sensititre STP7F, Gram Negative IVD AST recalledRemelOtherNationwide
DeviceCLASS IThermo Scientific, Sensititre CMC7AFLF, Gram Negative IVD AST recalledRemelOtherNationwide
DeviceCLASS IThermo Scientific, Sensititre MDRGN3F, Gram Negative IVD AST recalledRemelOtherNationwide
DeviceCLASS IThermo Scientific, Sensititre CMC5VGNF, Gram Negative IVD AST recalledRemelOtherNationwide
DeviceCLASS IThermo Scientific, Sensititre GN6F, Gram Negative IVD AST recalledRemelOtherNationwide
DeviceCLASS IThermo Scientific, Sensititre HPB1, Gram Negative IVD AST recalledRemelOtherNationwide
DeviceCLASS IThermo Scientific, Sensititre GN7F, Gram Negative IVD AST recalledRemelOtherNationwide
DeviceCLASS IThermo Scientific, Sensititre STP6F, Gram Negative IVD AST recalledRemelOtherNationwide
DeviceCLASS IIThermo Scientific Sensititre Gram Negative Susceptibility recalledRemelOtherNationwide
DeviceCLASS IIThermoScientific Oxoid Antimicrobial Susceptibility Discs recalledRemelPotency & AssayNationwide
DeviceCLASS IIBile Esculin Azide Agar w/ 6mcg/ml Vancomycin recalled by RemelRemelPackaging DefectsNationwide
DeviceCLASS IIHaemophilus Test Medium recalled by RemelRemelOtherNationwide
DeviceCLASS IIHaemophilus Test Medium recalled by RemelRemelOtherNationwide
DeviceCLASS IIBlood Agar/MacConkey Agar Bi-Plate recalled by RemelRemelDevice Malfunction8 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.