Biomerieux Inc: 197 recalls on record

Recalls filed with 1 agency: FDA (197).

First recall on record: October 17, 2012. Most recent: July 15, 2026.

Risk classification: Class I: 5 · Class II: 191 · Class III: 1

Most recent recalls

DateAgencyProduct
July 15, 2026FDAVITEK 2 AST-N447 TEST KIT Product reference 424620Z-2715-2026
February 11, 2026FDAVITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B (pb02n) o Ceftazidime…Z-1236-2026
May 1, 2024FDAVITEK 2 - AST Test kits (in vitro diagnostic test cards for antimicrobial susceptibility)…Z-1464-2024
January 11, 2023FDAVITEK MS CLINICAL REAGENT VITEK MS-DS, CATALOG 410893Z-0814-2023
January 11, 2023FDAVIDAS CLINICAL VIDAS RUB IGG 60 TESTS, CATALOG 30226Z-0797-2023
January 11, 2023FDAETEST CLINICAL ETEST MEROPENEM/VABORBACTAM MEV US S30, CATALOG 421560Z-0852-2023
January 11, 2023FDAVITEK 2 REAGENT AST-XN09 TEST KIT 20 CARDS, CATALOG 423425Z-0857-2023
January 11, 2023FDAETEST CLINICAL COLISTIN CO 256 US B100, CATALOG 537348Z-0863-2023
January 11, 2023FDAAPI LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300Z-0783-2023
January 11, 2023FDAPPM CLINICAL CRAPONNE CHROMID VRE 20 PLT US, CATALOG 43851Z-0803-2023
January 11, 2023FDAVITEK 2 REAGENT NH TEST KIT VTK2 20 CARDS, CATALOG 21346Z-0791-2023
May 18, 2022FDAVITEK 2 Systems and VITEK 2 with MYLA.Z-1059-2022
January 5, 2022FDAVIDAS RUB IgG (RBG), REF 30226Z-0432-2022
April 29, 2020FDAThe VITEK 2 Gram-positive Susceptibility Card is intended for use with the VITEK 2 System…Z-1742-2020
December 26, 2018FDAVITEK¿ 2 Systems Software Version 9.01 Update Kit.Z-0639-2019
October 31, 2018FDABACT/ALERT VIRTUO system, B Unit, with Version R2.0 Firmware Product Usage: The BacT/…Z-0229-2019
September 26, 2018FDAVITEK(R) 2 AST-P655, For susceptibility testing of Staphylococcus spp. Enterococcus spp.,…Z-3180-2018
August 29, 2018FDAbioMerieux VITEK 2 Gram Positive Cefoxitin Screen, VITEK 2 Gram Positive AST for Oxacilli…Z-2817-2018
July 18, 2018FDABioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usag…Z-2429-2018
September 27, 2017FDAVITEK(R) 2 GP, REF 21342, IVD, UDI 03573026131920, bioMerieux, Inc. VITEK(R) 2 is an aut…Z-3134-2017
September 6, 2017FDAVITEK¿ 2 Compact 15, REF numbers: 27415 and 27415R software and reagent cards designed f…Z-3075-2017
September 6, 2017FDAVITEK¿ 2 Compact 30, REF numbers: 27530 and 27530R (clinical), and 27630 and 17630R (ind…Z-3076-2017
August 2, 2017FDAVITEK 2 Gram Negative test kits containing colistin (cs01n)Z-2770-2017
July 19, 2017FDAVIDAS Testosterone, Ref 30418Z-2339-2017
June 21, 2017FDAVITEK¿ 2 Gram Negative Susceptibility card (AST-N359), IVD, REF 421573, 20 cards per car…Z-2522-2017

Questions about this company

How many recalls does Biomerieux Inc have?
Recalert has 197 U.S. recalls on record for Biomerieux Inc, published between October 17, 2012 and July 15, 2026.
What was the most recent Biomerieux Inc recall?
FDA recall Z-2715-2026, published July 15, 2026: VITEK 2 AST-N447 TEST KIT Product reference 424620
Which agencies have handled Biomerieux Inc recalls?
Biomerieux Inc appears as the recalling firm in recalls from: FDA (197).

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