PlainRecalls

Biomerieux Inc

Compiled from official public sources by the publisher.

422 recalls on record · Latest: Jul 15, 2026

Subscribe to new Biomerieux Inc recalls (RSS)

Agency notice ledger

Federal filing book Biomerieux Inc HEAVY-BOOK · SINGLE-AGENCY

#19 of 14,151 · 422 notices · 0.404% archive

  • BOOK 422 notices
  • RANK #19 of 14,151
  • SHARE 0.404% archive
  • AGENCY FDA Devices (422)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 15, 2026
  • PHOTO Olympus Corporation

Nearest notice-volume peer: Olympus Corporation of the Americas (8 notice gap)

Biomerieux Inc accounts for about 0.404% of the 104,423-notice archive on 422 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Biomerieux Inc compares to 14,151 recalling firms

Biomerieux Inc ranks 19th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Biomerieux Inc vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

422 19th of 14151 higher than 14,132 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Biomerieux Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Biomerieux Inc holds about 0.404% of archive notices alongside 422 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 15, 2026

VITEK 2 AST-N447 TEST KIT Product reference 424620
FDA Devices Moderate Feb 11, 2026

VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B (pb02n) o Ceftazidime/avibactam (cza02n) o Meropenem/Vaborbactam (mev01n) o Imipenem (ipm05n) o Imipenem/Relebactam (ipr01n); CARD NAME/ PRODUCT REFERENCE: AST-N399 423701 AST-N402 423644 AST-N403 423645 AST-N404 423664 AST-N405 423864 AST-N406 423869 AST-N407 423870 AST-N409 423925 AST-N412 423936 AST-N413 423928 AST-N414 423933 AST-N415 423934 AST-N416 423935 AST-N417 423880 AST-N419
FDA Devices Moderate Oct 8, 2025

VITEK¿ 2 Gram-negative AST Test Kits (Cards) containing Colistin formulation cs02n. VITEK¿ 2 is an automated system consisting of instruments, software and reagent cards designed for the identification and antimicrobial susceptibility testing of bacteria and yeast. Export only
FDA Devices Critical May 1, 2024

VITEK 2 - AST Test kits (in vitro diagnostic test cards for antimicrobial susceptibility): a) AST-N334, REF 418984; b) AST-GN95, REF 421982; c) AST-GN99, REF 423102; d) AST-N390, REF 423340; e) AST-N391, REF 423341; f) AST-N392, REF 423342; g) AST-N395, REF 423491; h) AST-N401, REF 423643; i) AST-N402, REF 423644; j) AST-N404, REF 423664; k) AST-N802, REF 423706; l) AST-N405, REF 423864; m) AST-N417, REF 423880; n) AST-N408, REF 423924; o) AST-N409, REF 423925; p
FDA Devices Moderate Mar 8, 2023

MYLA comprises AST Filters in conjunction with VITEK MS; middleware which connects microbiology laboratory instruments for ID/AST and blood culture activities and the laboratory information system (LIS).
FDA Devices Moderate Jan 11, 2023

PPM LOMBARD PRODUCTS TSA 10PLT, CATALOG M1040
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS LISTERIA 60T, CATALOG 30700
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS HCG 60 TESTS, CATALOG 30405-01
FDA Devices Moderate Jan 11, 2023

PPM INDUSTRY COMBOURG CHROMID CARBA US 20 PLT, CATALOG 414012
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN80 TEST KIT 20 CARDS, CATALOG 413437
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL AMIKACIN AK 256 US S30, CATALOG 412218
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL RIFAMPICIN RI 32 US S30, CATALOG 412449
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-N801 TEST KIT 20 CARDS, CATALOG 423416
FDA Devices Moderate Jan 11, 2023

BIOBALL B.SPIZIZENII NCTC 10400 550X20, CATALOG 56012
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL MEROPENEM MP 32 US S30, CATALOG 412401
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL ERAVACYCLINE ERV US S30, CATALOG 421553
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL COLISTIN CO 256 US B100, CATALOG 537348
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL ETEST MEROPENEM/VABORBACTAM MEV US S30, CATALOG 421560
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS RUB IGG 60 TESTS, CATALOG 30226
FDA Devices Moderate Jan 11, 2023

PPM CLINICAL CRAPONNE CHROMID VRE 20 PLT US, CATALOG 43851
FDA Devices Moderate Jan 11, 2023

API LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT NH TEST KIT VTK2 20 CARDS, CATALOG 21346
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-XN09 TEST KIT 20 CARDS, CATALOG 423425
FDA Devices Moderate Jan 11, 2023

VITEK MS CLINICAL REAGENT VITEK MS-DS, CATALOG 410893
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GP78 TEST KIT 20 CARDS, CATALOG 421051
FDA Devices Moderate Jan 11, 2023

PPM LOMBARD PRODUCTS IRR COUNT-TACT 3P AGAR 100 PLT, CATALOG 418049
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL ETEST MEROPENEM MP M100 US, CATALOG 423786
FDA Devices Moderate Jan 11, 2023

PPM CLINICAL CHROMID MRSA 20 PLT US, CATALOG 43841
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL CEFTAZIDIM/AVIBACTAM US S30, CATALOG 419046
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN79 TEST KIT 20 CARDS, CATALOG 413436
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL MINOCYCLINE MC 256 US S30, CATALOG 412407
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS SALMONELLA 60T, CATALOG 30702
FDA Devices Moderate Jan 11, 2023

PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT, CATALOG 423723
FDA Devices Moderate Jan 11, 2023

TEMPO REAGENTS TEMPO CONTROL KIT , CATALOG 80000
FDA Devices Moderate Jan 11, 2023

API 20 C AUX 25 STRIPS+25 MEDIA, CATALOG 20210
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN81 TEST KIT 20 CARDS, CATALOG 413438
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GP75 TEST KIT 20 CARDS, CATALOG 415670
FDA Devices Moderate Jan 11, 2023

PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT, CATALOG 419014
FDA Devices Moderate Jan 11, 2023

PPM CLINICAL CRAPONNE CLINICAL CHROMID CANDIDA 20 PLATES, CATALOG 43631
FDA Devices Moderate Jan 11, 2023

PPM LOMBARD PRODUCTS CT&TI-TSA + L & P80 10PLT, CATALOG C6045-TI
FDA Devices Moderate Jan 11, 2023

GENE-UP REAGENT GENE-UP Salmonella 2, CATALOG 423105
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL CEFTRIAXONE TX 32 US S30, CATALOG 412302
FDA Devices Moderate Jan 11, 2023

PPM LOMBARD PRODUCTS R2A MEDIUM 10PLT, CATALOG M1065
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL QCV-QUALITY CONTROL VIDAS 60T, CATALOG 30706
FDA Devices Moderate Jan 11, 2023

PPM INDUSTRY COMBOURG LPT BROTH (4X3L), CATALOG 410849
FDA Devices Moderate Jan 11, 2023

PPM CLINICAL CHROMID MRSA S AUREUS 20PLT US, CATALOG 414524
FDA Devices Moderate Jan 11, 2023

GENE-UP REAGENT GENE-UP LYSIS KIT, CATALOG 414057
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL IMIPENEM IP 32 US S30, CATALOG 412373
FDA Devices Moderate Jan 11, 2023

PREVI COLOR GRAM REAGENT NOZZLE CLEANING SOLUTION (NA), CATALOG 29588
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-ST02 TEST KIT 20 CARDS, CATALOG 420915

Biomerieux Inc carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Olympus Corporation of the Americas 414 Baxter Healthcare Corporation 413 Philips North America Llc 404 B Braun Medical Inc 444

Frequently Asked Questions

How many federal recall notices name Biomerieux Inc? ▼
PlainRecalls indexes 422 distinct federal recall events naming Biomerieux Inc, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Biomerieux Inc sit among other recalling firms? ▼
Biomerieux Inc ranks #19 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Biomerieux Inc's notices? ▼
FDA Devices accounts for 422 of this firm's 422 indexed notices.
What product category dominates Biomerieux Inc's filing book? ▼
Filings for Biomerieux Inc span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Biomerieux Inc: 422 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Biomerieux Inc; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026