Biomerieux Inc
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
- B Braun Medic…
B Braun Medical Inc
444 notices
- Biomerieux Inc (this)
Biomerieux Inc
422 notices
- Olympus Corpo…
Olympus Corporation of the Americas
414 notices
- Baxter Health…
Baxter Healthcare Corporation
413 notices
- Fresh Ideatio…
Fresh Ideation Food Group, LLC dba Fresh Creative Cuisine
409 notices
- Philips North…
Philips North America Llc
404 notices
What this shows Biomerieux Inc holds about 0.404% of archive notices alongside 422 distinct filings.
FDA Devices Moderate Jun 21, 2017
VITEK 2 Gram-Positive identification card (GP), IVD, REF 21342, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N213), REF 413063, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-GN73), REF 413404, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N271), REF 414163, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N237), REF 413172, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Fungal Susceptibility card (AST-YS01), REF 22108, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N215), REF 413065, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram-Negative identification card (GN), IVD, REF 21341, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-GN75), REF 413432, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N208), IVD, REF 413062, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N238), REF 413203, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N204), REF 412865, 20 cards per carton. .
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-GN81), REF 413438, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N209), REF 412938, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-GN87), REF 413943, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N233), REF 413117, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N320), IVD, REF 418204, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N352), IVD, REF 421258, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Positive Susceptibility card (AST-P640), IVD, REF 418579, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Streptococcus Susceptibility card (AST-ST03), IVD, REF 421040, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N324), IVD, REF 418603, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N272), REF 414164, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N354), IVD, REF 421350, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-GN04), IVD, REF 22000, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N286), REF 414778, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N363), IVD, REF 421692, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-GN82), REF 413439, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N315), IVD, REF 417426, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N285), REF 414740, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Positive Susceptibility card (AST-P644), IVD, REF 418673, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Positive Susceptibility card (AST-P621), REF 412533, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Positive Susceptibility card (AST-GP71), REF 410750, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N217), REF 413080, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N292), REF 415063, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Positive Susceptibility card (AST-P606), REF 22330, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Positive Susceptibility card (AST-P629), REF 414576, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N350), IVD, REF 421037, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Positive Susceptibility card (AST-P603), REF 22320, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N211), REF 413043, 20 cards per carton.
FDA Devices Moderate Jun 21, 2017
VITEK¿ 2 Gram Negative Susceptibility card (AST-N293), REF 415369, 20 cards per carton.
FDA Devices Critical May 18, 2016
Vitek 2 Gram Positive Susceptibility Test Cards (AST-P640 REF 418579), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed in the Product Information manual.
FDA Devices Critical May 18, 2016
Vitek 2 Gram Positive Susceptibility Test Cards (AST-P645 REF 419602), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed in the Product Information manual.
FDA Devices Critical May 18, 2016
Vitek 2 Gram Positive Susceptibility Test Cards (AST-P639 REF 418662), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed in the Product Information manual.
FDA Devices Critical May 18, 2016
Vitek 2 Gram Positive Susceptibility Test Cards (AST-P644 REF 418673), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed in the Product Information manual.
FDA Devices Critical May 18, 2016
Vitek 2 Gram Positive Susceptibility Test Cards (AST-P642 REF 418604), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed in the Product Information manual.
FDA Devices Critical May 18, 2016
Vitek 2 Gram Positive Susceptibility Test Cards (AST-P646 REF 420144), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed in the Product Information manual.
FDA Devices Critical May 18, 2016
Vitek 2 Gram Positive Susceptibility Test Cards (AST-P636 REF 417951), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed in the Product Information manual.
FDA Devices Critical May 18, 2016
Vitek 2 Gram Positive Susceptibility Test Cards (AST-P641 REF 418590), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed in the Product Information manual.
FDA Devices Critical May 18, 2016
Vitek 2 Gram Positive Susceptibility Test Cards (AST-P643 REF 418671), 20 cards/kit. Product Usage: The VITEK 2 Gram Positive Susceptibility Card is intended for use with VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents when used as instructed in the Product Information manual.
FDA Devices Moderate May 11, 2016
VITEK 2 Gram Positive Susceptibility Test Cards (AST-P605), REF 22 325. 20 Cards/Kit. bioMerieux, Inc, Durham, North Carolina 27712. 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. The VITEK 2 utilizes growth-based biochemical patterns to determine identification. The VITEK 2 provides minimal inhibitory concentration (MIC) results for most organism/drug combinati
Biomerieux Inc carries an outsized archive share
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (422 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
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