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 446 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 101,704 records spanning 1995 through the present, FDA Medical Devices accounts for roughly 38.4% 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 1 critical (Class I-equivalent) actions, 48 moderate recalls, and 1 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 Jun 13, 2018 to Jun 20, 2018, covering 15 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).
The VITEK 2 Gram-Positive identification card (GP) is intended for use with the VITEK 2 Systems for the automated identification of most significant …
BioMerieux SA
Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG, Catalog Number 45-871
Angiodynamics Inc. (Navilyst Medical Inc.)
XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124
Angiodynamics Inc. (Navilyst Medical Inc.)
Bio-Stable 5F SL-55CM IR-145 Kit Valved with Nitinol GW PG, Catalog Number 45-882
Angiodynamics Inc. (Navilyst Medical Inc.)
Bio-Stable 5F DL-55CM IR-145 Kit Non-Valved with Nitinol GW PG, Catalog Number 45-887
Angiodynamics Inc. (Navilyst Medical Inc.)
RS 5F DL XPP KIT, Catalog Number 60M183104
Angiodynamics Inc. (Navilyst Medical Inc.)
Accu-Chek Aviva Plus Test Strip, Blood glucose monitoring system, Catalog nos. 06908217001, 06908268001, 06908349001,06908217001 Product Usage: T…
Roche Diabetes Care, Inc.
Accu-Chek Inform II Test Strip, Whole blood glucose test system, Catalog no. 05942861001 Product Usage: The Accu-Chek Inform II test strips are f…
Roche Diabetes Care, Inc.
12C
Ion Beam Applications S.A.
lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls (High 125 ng/ml and Low 75 ng/ml) are used as control materials in the ammonolysis ED…
Alere San Diego Inc. DBA Immunalysis Corporation
The VITEK 2 Neisseria-Haemophilus identification card (NH) is intended for use with the VITEK 2 Systems for the automated identification of most clin…
BioMerieux SA
Bio-Stable 5F SL-55CM MST-70 Kit Valved with Nitinol Guidewire PG, Catalog Number 45-892
Angiodynamics Inc. (Navilyst Medical Inc.)
Proteus 235 The PTS is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and ot…
Ion Beam Applications S.A.
The VITEK 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems in clinical laboratories as an in vitro test to determine …
BioMerieux SA
Oxidase Reagent (ref: 55635): This test is used to detect the production of the enzyme cytochrome oxidase by bacteria. This enzyme is characteristic …
BioMerieux SA
CAN 5F DL BIOFLO PASV PICC NURSING TRAY, Catalog Number 60M700936
Angiodynamics Inc. (Navilyst Medical Inc.)
Brilliance 64 with DEPMED HARDENING KIT 12NC: 459800191351, Model Number 728231. Computed Tomography X-ray system
Philips Medical Systems (Cleveland) Inc
RS 5F DL BIOFLO PASV, Catalog Number 60M183481
Angiodynamics Inc. (Navilyst Medical Inc.)
RS - TANDEM 5F DL BIOFLO MIDLINE, Catalog Number 60M035472
Angiodynamics Inc. (Navilyst Medical Inc.)
RS TANDEM 5F DL BIOFLO PASV, Catalog Number 60M232242
Angiodynamics Inc. (Navilyst Medical Inc.)
Bio-Stable 5F SL-55CM IR-145 Kit Valved PG, Catalog Number 45-818
Angiodynamics Inc. (Navilyst Medical Inc.)
MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, BAG RESERVOIR, FILTER, CO2 AND 7 FT. OXYGEN TUBING, REF CPRM1116FC
Sun Med, LLC
The PREVI¿ Color Gram dyes are used with the PREVI¿ Color Gram instrument to stain bacterial and fungal microorganisms for direct examination, accord…
BioMerieux SA
RS 5F DL XCELA PICC, Catalog Number 60M122272
Angiodynamics Inc. (Navilyst Medical Inc.)
IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 867146
Philips Electronics North America Corporation
Color Gram 2 (COLOR GRAM 2 - F), these stains are used to stain bacterial and fungal microorganisms for direct examination, according to the Gram met…
BioMerieux SA
MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, CO2 AND 7 FT. OXYGEN TUBING, REF CPRM1126C
Sun Med, LLC
MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, FILTER, PEEP VALVE, CO2 AND 7 FT. OXYGEN TUBING, REF CPRM1126FPC
Sun Med, LLC
BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit PG, Catalog Number 75-019
Angiodynamics Inc. (Navilyst Medical Inc.)
TANDEM 5F DL BIOFLO PASV, Catalog Number 60M140567
Angiodynamics Inc. (Navilyst Medical Inc.)
Bio-Stable 5F SL-55CM IR-145 Kit Non-Valved with Nitinol GW PG, Catalog Number 45-886
Angiodynamics Inc. (Navilyst Medical Inc.)
RS TANDEM 5F DL BIOFLO PASV, Catalog Number 60M120196
Angiodynamics Inc. (Navilyst Medical Inc.)
BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol Wire PG, Catalog Number 75-038
Angiodynamics Inc. (Navilyst Medical Inc.)
Vanguard Knee System PS Tibial Bearing, Part Number 183621 Intended for use in knee joint replacement procedures.
Zimmer Biomet, Inc.
MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1126P
Sun Med, LLC
IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865351
Philips Electronics North America Corporation
RS 5F DL XPP, Catalog Number 60M030393
Angiodynamics Inc. (Navilyst Medical Inc.)
Part #: SAM XT-C, Model: Hi-Viz Orange or Civilian
The Seaberg Company Inc
Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved with Nitinol Guidewire PG, Catalog Number 45-895
Angiodynamics Inc. (Navilyst Medical Inc.)
BioFlo PICC (NV) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol Wire PG, Catalog Number 75-033
Angiodynamics Inc. (Navilyst Medical Inc.)
RS TANDEM 5F DL BIOFLO PICC, Catalog Number 60M250097
Angiodynamics Inc. (Navilyst Medical Inc.)
Aortic Arterial Cannula 24 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002267, Article Number A24-7107. For use in cardiop…
Maquet Cardiopulmonary Ag
RS 5F DL BIOFLO PASV, Catalog Number 60M161567
Angiodynamics Inc. (Navilyst Medical Inc.)
STAT-Check MANUAL RESUSCITATOR / VENTILATOR, REF SC9200MBP-1
Sun Med, LLC
Microintroducer Kit, 5F, Tearaway Sheath/Dilator PG, Catalog Number 45-901
Angiodynamics Inc. (Navilyst Medical Inc.)
Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM, D 2.7MM, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Part Number: 000-K-011C
Orthofix, Inc
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), infusion pump, 35700BAX2 Product Usage: The Baxter SIGMA Spectrum Infus…
Baxter Healthcare Corporation
Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a physician s supervision / directio…
Draeger Medical Systems, Inc.
ST-AIA PACK Testosterone; Part Number: 025204 Assay, Reproductive Hormone
Tosoh Bioscience Inc
Y-Plate, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Size (Part Number): a) Small (003-C-01001); b) Large (003-C-02001)
Orthofix, Inc
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
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recall counts and figures reflect FDA Medical Devices's own published filings, aggregated alongside the other two federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.