PlainRecalls

Biomerieux Inc

Compiled from official public sources by the publisher.

422 recalls on record · Latest: Jul 15, 2026

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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 · 2026-09-14

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 Jan 11, 2023

VITEK 2 REAGENT AST-GN99 TEST KIT 20 CARDS, CATALOG 423102
FDA Devices Moderate Jan 11, 2023

API NIT1 NIT2 REAGENTS, CATALOG 70442
FDA Devices Moderate Jan 11, 2023

BIOBALL A.BRASILIENSIS NCPF 2275 550X20, CATALOG 56011
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL TOBRAMYCIN TM 256 US S30, CATALOG 412478
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-XN15 TEST KIT 20 CARDS, CATALOG 423829
FDA Devices Moderate Jan 11, 2023

PPM CLINICAL CHROMID STREPTO B US 20 PLT, CATALOG 419751
FDA Devices Moderate Jan 11, 2023

BIOBALL K.RHIZOPHILA (30X20), CATALOG 412690
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN70 TEST KIT 20 CARDS, CATALOG 413401
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL VANCOMYCIN VA 256 US S30, CATALOG 412486
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345
FDA Devices Moderate Jan 11, 2023

VITEK MS CLINICAL REAGENT VITEK MS-CHCA, CATALOG 411071
FDA Devices Moderate Jan 11, 2023

PPM CLINICAL CRAPONNE CHROMID C.DIFFICILE 20 PLT, CATALOG 43871
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL ETEST VANCOMYCIN VA M100 US, CATALOG 423788
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GP67 TEST KIT 20 CARDS, CATALOG 22226
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL IMIPENEM RELEBACTAM IPR US S30, CATALOG 420927
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS ESTRADIOL II 60 TESTS, CATALOG 30431-01
FDA Devices Moderate Jan 11, 2023

PPM INDUSTRY COMBOURG BACARA 20PLATES 90MM, CATALOG AEB520100
FDA Devices Moderate Jan 11, 2023

API VP1 VP2 REAGENTS, CATALOG 70422
FDA Devices Moderate Jan 11, 2023

PPM LOMBARD PRODUCTS T PHOSPHATE BUFFERSTERILE 20X9ML, CATALOG T8035
FDA Devices Moderate Jan 11, 2023

API JAMES 2AMP, CATALOG 70542
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412240
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN69 TEST KIT 20 CARDS, CATALOG 413400
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS LH 60 TESTS, CATALOG 30406-01
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL BENZYLPENICIL PG 256 US S30, CATALOG 412262
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT GN TEST KIT VTK2 20 CARDS, CATALOG 21341
FDA Devices Moderate Jan 11, 2023

ASTUTE REAGENT NEPHROCHECK LIQUID CONTROLS KIT US, CATALOG 500013
FDA Devices Moderate Jan 11, 2023

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

PPM LOMBARD PRODUCTS IR&DB - TSA (32ML) 10PLT, CATALOG M1205-IR
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331
FDA Devices Moderate Jan 11, 2023

BIOBALL P.AERUGINOSA NCTC 12924 550X20, CATALOG 56017
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL FLUCONAZOLE FL 256 US S30, CATALOG 412333
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL ERYTHROMYCIN EM 256 US S30, CATALOG 412333
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL LEVOFLOXACIN LE 32 US S30, CATALOG 412392
FDA Devices Moderate Jan 11, 2023

VITEK MS CLINICAL REAGENT VITEK MS-FA, CATALOG 411072
FDA Devices Moderate Jan 11, 2023

PREVI COLOR GRAM REAGENT IODINE-B (NA), CATALOG 29586
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN95 TEST KIT 20 CARDS, CATALOG 421982
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT YST TEST KIT VTK2 20 CARDS, CATALOG 21343
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT GP TEST KIT VTK2 20 CARDS, CATALOG 21342
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412252
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS MEASLES IGG 60TESTS, CATALOG 30219
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICALVIDAS VARICEL. ZOSTER IGG 60 T, CATALOG 30217
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS BRAHMS PROCALCITONIN 60T, CATALOG 30450-01
FDA Devices Moderate Jan 11, 2023

ASTUTE REAGENT ASTUTE ELECTRONIC QUALITY CTRL DEVICE US, CATALOG 400016
FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL CEFTOLOZANE/TAZO C/T US S30, CATALOG 414445
FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN73 TEST KIT 20 CARDS, CATALOG 413404
FDA Devices Moderate Jan 11, 2023

DCOUNT SYSTEMS REAGENTS CHEMCHROME V14 (6X1.8ML), CATALOG 306-R1026-01
FDA Devices Moderate Jan 11, 2023

API 20 E 25 STRIPS, CATALOG 20100
FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS PROGESTERONE 60 TESTS, CATALOG 30409-01
FDA Devices Moderate Jan 11, 2023

API STAPH 25 STRIPS+25 MEDIA, CATALOG 20500
FDA Devices Moderate Oct 5, 2022

VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx.

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