FDA Medical Devices
All recall actions attributed to FDA Medical Devices in our federal database. Each record links back to the agency's official notice so you can verify status, remedy, and amendments before acting.
U.S. Food and Drug Administration — Medical device recalls
39,096 recalls · Page 200 of 782
FDA Medical Devices Recall Insight
PlainRecalls tracks 39,096 recall actions attributed to the FDA Medical Devices in our federal recall index. Across the full PlainRecalls database of 100,165 records spanning 1995 through the present, FDA Medical Devices accounts for roughly 39.0% of all indexed recalls. The agency's stated scope — U.S. Food and Drug Administration — Medical device recalls — determines what classes of products flow through its recall pipeline and how quickly notices reach consumers. With 782 pages of records at 50 recalls per page, this archive represents one of the longest continuous federal enforcement histories accessible to the public.
Looking at the 50 records on this page alone, the severity distribution skews toward 0 critical (Class I-equivalent) actions, 50 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 50 disclose a unit count — the gap reflects regulatory filing norms where firms disclose lot numbers or distribution channels instead of absolute quantities. This page spans recalls from Jan 11, 2023 to Jan 11, 2023, covering 8 distinct firms. Severity mix is a leading indicator: a page weighted toward critical classifications usually signals an active public-health concern, while lower-severity clusters often represent labeling, undeclared-allergen, or minor design corrections.
Agency-level browsing is useful when a defect pattern crosses categories — for example, a supplier contamination can trigger dozens of downstream recalls that share no obvious product tag but a single issuing agency. Use the pagination below to scan the full archive, or combine this agency filter with category and manufacturer views elsewhere on PlainRecalls to intersect the data. Recall records are sourced directly from FDA Medical Devices's public enforcement feeds and are updated as the agency publishes new notices; the federal record is the authoritative version, and this page aggregates what the agency itself has released. For high-stakes decisions — medical, automotive, or childcare — always click through to the recall detail page and cross-verify the recall number against the agency's current site. Record counts reflect all indexed actions regardless of status (ongoing, terminated, or completed).
BIOBALL A.BRASILIENSIS NCPF 2275 550X20, CATALOG 56011
Biomerieux Inc
ETEST CLINICAL TOBRAMYCIN TM 256 US S30, CATALOG 412478
Biomerieux Inc
VITEK 2 REAGENT AST-XN15 TEST KIT 20 CARDS, CATALOG 423829
Biomerieux Inc
PPM CLINICAL CHROMID STREPTO B US 20 PLT, CATALOG 419751
Biomerieux Inc
BIOBALL K.RHIZOPHILA (30X20), CATALOG 412690
Biomerieux Inc
VITEK 2 REAGENT AST-GN70 TEST KIT 20 CARDS, CATALOG 413401
Biomerieux Inc
VERIFY Dual Species Self-Contained Biological Indicators, 100 per box Item Number: S3061 Intended for use in installation testing and routine mon…
Steris Corporation
ETEST CLINICAL VANCOMYCIN VA 256 US S30, CATALOG 412486
Biomerieux Inc
VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345
Biomerieux Inc
VITEK MS CLINICAL REAGENT VITEK MS-CHCA, CATALOG 411071
Biomerieux Inc
Liquid Assayed Specific Protein- In vitro diagnostic use, in the quality control of serum on clinical chemistry and immunoassay systems Catalog Numb…
Randox Laboratories Ltd.
Detect Covid-19 Test Product/Model Number: 21205
Detect Headquarters
Guardian iOS app (MMT-8200) and Guardian Android app (MMT-8201), part of the Guardian 4 system
Medtronic MiniMed
PPM CLINICAL CRAPONNE CHROMID C.DIFFICILE 20 PLT, CATALOG 43871
Biomerieux Inc
ETEST CLINICAL ETEST VANCOMYCIN VA M100 US, CATALOG 423788
Biomerieux Inc
DeRoyal Tonsillectomy Tray, REF 89-10698.01
DeRoyal Industries Inc
BECKMAN COULTER IRISpec CA/CB/CC control, REF 900-7211, For in vitro diagnostic use only.
Beckman Coulter, Inc.
VITEK 2 REAGENT AST-GP67 TEST KIT 20 CARDS, CATALOG 22226
Biomerieux Inc
ETEST CLINICAL IMIPENEM RELEBACTAM IPR US S30, CATALOG 420927
Biomerieux Inc
VIDAS CLINICAL VIDAS ESTRADIOL II 60 TESTS, CATALOG 30431-01
Biomerieux Inc
PPM INDUSTRY COMBOURG BACARA 20PLATES 90MM, CATALOG AEB520100
Biomerieux Inc
API VP1 VP2 REAGENTS, CATALOG 70422
Biomerieux Inc
PPM LOMBARD PRODUCTS T PHOSPHATE BUFFERSTERILE 20X9ML, CATALOG T8035
Biomerieux Inc
API JAMES 2AMP, CATALOG 70542
Biomerieux Inc
ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412240
Biomerieux Inc
VITEK 2 REAGENT AST-GN69 TEST KIT 20 CARDS, CATALOG 413400
Biomerieux Inc
VIDAS CLINICAL VIDAS LH 60 TESTS, CATALOG 30406-01
Biomerieux Inc
ETEST CLINICAL BENZYLPENICIL PG 256 US S30, CATALOG 412262
Biomerieux Inc
VITEK 2 REAGENT GN TEST KIT VTK2 20 CARDS, CATALOG 21341
Biomerieux Inc
ASTUTE REAGENT NEPHROCHECK LIQUID CONTROLS KIT US, CATALOG 500013
Biomerieux Inc
PPM LOMBARD PRODUCTS CT&IR&DB-TSA + L & P80 10PLT, CATALOG C6045-IR
Biomerieux Inc
PPM LOMBARD PRODUCTS IR&DB - TSA (32ML) 10PLT, CATALOG M1205-IR
Biomerieux Inc
ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331
Biomerieux Inc
BIOBALL P.AERUGINOSA NCTC 12924 550X20, CATALOG 56017
Biomerieux Inc
ETEST CLINICAL FLUCONAZOLE FL 256 US S30, CATALOG 412333
Biomerieux Inc
ETEST CLINICAL ERYTHROMYCIN EM 256 US S30, CATALOG 412333
Biomerieux Inc
Liquid Assayed Specific Protein Control Level 3- In vitro diagnostic use, in the quality control of serum on clinical chemistry and immunoassay syste…
Randox Laboratories Ltd.
ETEST CLINICAL LEVOFLOXACIN LE 32 US S30, CATALOG 412392
Biomerieux Inc
VITEK MS CLINICAL REAGENT VITEK MS-FA, CATALOG 411072
Biomerieux Inc
PREVI COLOR GRAM REAGENT IODINE-B (NA), CATALOG 29586
Biomerieux Inc
VITEK 2 REAGENT AST-GN95 TEST KIT 20 CARDS, CATALOG 421982
Biomerieux Inc
VITEK 2 REAGENT YST TEST KIT VTK2 20 CARDS, CATALOG 21343
Biomerieux Inc
VITEK 2 REAGENT GP TEST KIT VTK2 20 CARDS, CATALOG 21342
Biomerieux Inc
ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412252
Biomerieux Inc
VIDAS CLINICAL VIDAS MEASLES IGG 60TESTS, CATALOG 30219
Biomerieux Inc
VITROS Immunodiagnostic Products Intact PTH Reagent Pack- IVD For the quantitative measurement of intact parathyroid hormone (iPTH) in human serum a…
Ortho-Clinical Diagnostics, Inc.
VIDAS CLINICALVIDAS VARICEL. ZOSTER IGG 60 T, CATALOG 30217
Biomerieux Inc
VIDAS CLINICAL VIDAS BRAHMS PROCALCITONIN 60T, CATALOG 30450-01
Biomerieux Inc
ASTUTE REAGENT ASTUTE ELECTRONIC QUALITY CTRL DEVICE US, CATALOG 400016
Biomerieux Inc
VERIFY Steam Test Pack (20 Tests and 5 controls) Item Number: S3065 Intended for use in installation testing and routine monitoring of steam and …
Steris Corporation
Nearby Agencies
Explore recalls from other federal agencies that share oversight of product safety.
Learn More About Recalls
Disclaimer: This information is provided for informational purposes only and does not constitute professional advice. Consult a qualified professional before making decisions based on this data.
- Source: FDA Medical Devices — verify with the issuing agency: official recall page →
- Source: PlainRecalls Data Index — aggregated from FDA openFDA, CPSC, and NHTSA public databases
Read our methodology — how this data is sourced, computed, and verified.