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 375 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 3 critical (Class I-equivalent) actions, 46 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 Aug 21, 2019 to Aug 28, 2019, covering 17 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).
Kit BD Max Enteric Viral Panel EU Catalog # 443985
Becton Dickinson & Co.
BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 368056
Becton Dickinson & Company
MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643
Siemens Medical Solutions USA, Inc
BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection Tubes, Catalog Number 367962
Becton Dickinson & Company
Kit BD Max ExK TNA 2; Catalog # 442825
Becton Dickinson & Co.
Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (23mm) 9630TF23 UDI:00690103201246
Edwards Lifesciences, LLC
Kit BD Max ExK DNA 1 EU LUO; Catalog # 442818
Becton Dickinson & Co.
PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery Pack, 40 Pouches - PDBP-040-2 …
Pro-Dex Inc
Kit BD Max MRSA; Catalog # 442953
Becton Dickinson & Co.
IMMULITE 1000 Progesterone, Model LKPW1, SMN Number 10381128
Siemens Healthcare Diagnostics, Inc.
ACUSON NX3 Diagnostic Ultrasound System, Model # 11235612, RX Only, Siemens Medical Solutions, containing software versions: VA10A, VA10B, VA10C, V…
Siemens Medical Solutions USA, Inc.
Kit BD Max Vaginal Panel; Catalog # 443712
Becton Dickinson & Co.
Kit BD Max ExK DNA 2 EU LUO; Catalog # 442820
Becton Dickinson & Co.
Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 For In Vitro Diagnostic Use in clinical laboratories. Scanner Label/Labeling…
Luminex Corporation
MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582
Siemens Medical Solutions USA, Inc
Kit BD Max StaphSR; Catalog # 443419
Becton Dickinson & Co.
BD Vacutainer LH (Lithium Heparin) 68 I.U. Plus Blood Collection Tubes, Catalog Number 368884
Becton Dickinson & Company
ACUSON NX3 Elite Diagnostic Ultrasound System, Model # 11235411, RX Only, Siemens Medical Solutions, containing software versions: VA10A, VA10B, VA…
Siemens Medical Solutions USA, Inc.
ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software version VA10A, VA10B, VA11A, VA11…
Siemens Medical Solutions USA, Inc.
MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915
Siemens Medical Solutions USA, Inc
Kit BD Max CT/GC/TV; Catalog # 442970
Becton Dickinson & Co.
Thoratec HeartMate 3 LVAS Implant Kit, Sterile, REF 106524/106524US, RX only, Left Ventricular Assist System
Thoratec Corp.
Kit BD Max Cdiff EU; Catalog # 442555
Becton Dickinson & Co.
MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914
Siemens Medical Solutions USA, Inc
Luer Lock Set - Catalog # MPC-125, for IV administration sets.
Molded Products Inc
BD Vacutainer Lithium HeparinN 75 USP Units Blood Collection Tubes, Catalog Number 367884
Becton Dickinson & Company
Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (26mm) 9630TF26 UDI:00690103201253
Edwards Lifesciences, LLC
TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-tip extens…
TiSport, Llc
ABL90 FLEX Analyzer REF 393090 UDI:05700693930909
Radiometer America Inc
Kit BD Max GC RT PCR Assay; Catalog # 443486
Becton Dickinson & Co.
BD Vacutainer LH (Lithium Heparin) 102 I.U. Plus Blood Collection Tubes, Catalog Number 368886
Becton Dickinson & Company
BD Vacutainer PST Blood Collection Tubes, Catalog Number 368035, 368036
Becton Dickinson & Company
Kit BD Max Enteric Parasite Panel EU; Catalog # 442960
Becton Dickinson & Co.
BD Vacutainer Lithium HeparinN (LH) 158 USP Units Blood Collection Tubes, Catalog Number 367880
Becton Dickinson & Company
N Cuvette Segments for BN ProSpec System-IVD a system for the quantitative determination of proteins in serum, plasma, urine and CSF. Siemens Materi…
Siemens Healthcare Diagnostics, Inc.
Kit BD Max ExK DNA 2 USA; Catalog # 442819
Becton Dickinson & Co.
BD Vacutainer PST Gel and Lithium HeparinN (LH) Blood Collection Tubes, Catalog Number 367963
Becton Dickinson & Company
ZYMUTEST HIA MonoStrip, IgGAM ELISA kit, Model No. RK041D, for in vitro diagnostic use.
Aniara Diagnostica LLC
Kit BD Max Enteric Bacterial Panel EU; Catalog # 442963
Becton Dickinson & Co.
BD Vacutainer PST Gel and Lithium HeparinN (LH) 65 Units Blood Collection Tubes, Catalog Number 367961
Becton Dickinson & Company
IMMULITE 2000 Progesterone; Models US: L2KPW2, L2KPW6 and OUS: L2KPW2(D), L2KPW6(D); SMN Numbers US: 10901873, 10901874 and OUS 10381181, 10381170
Siemens Healthcare Diagnostics, Inc.
Kit BD Max MRSA XT; Catalog # 443461
Becton Dickinson & Co.
Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (20 mm) 9630TF20 UDI:00690103201239
Edwards Lifesciences, LLC
MICRO-TEMP LT System, Model 749- Localized Heat Therapy System is intended to warm a patient's body part through conductive heat transfer.
Cincinnati Sub-Zero Products LLC, a Gentherm Company
DeRoyal Enteral Safe Feeding Tubes: a) REF 54-2450R, 5 FR x 24" Polyurethane b) REF 54-2465R, 6.5 FR x 24" Polyurethane c) REF 54-2480R, 8 FR x 24…
DeRoyal Industries Inc
Go-EZ Screw 6.5x120, Item Number 19672 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for va…
BioPro, Inc.
K-Wire Single Trocar 2.5x150mm, Item Number OL15025S - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is i…
BioPro, Inc.
Go-EZ Screw 6.5x34, Item Number 19653 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for var…
BioPro, Inc.
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812
Zimmer Biomet, Inc.
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811
Zimmer Biomet, Inc.
Nearby Agencies
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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.