PlainRecalls

Biomerieux Inc

Compiled from official public sources by the editorial team.

421 recalls on record · Latest: Feb 11, 2026

Biomerieux Inc Recall Insight

Biomerieux Inc appears on 421 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.414% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Feb 11, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 49 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Sep 7, 2022 to Jan 11, 2023.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

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.

FDA Devices Moderate Sep 7, 2022

VITEK 2 / MYLA VITEK 2 Software versions 8.01, 8.02 (veterinary use only), 9.01, 9.02, 9.03 MYLA Software versions V4.8 and V4.9

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.