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 238 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 4 critical (Class I-equivalent) actions, 42 moderate recalls, and 4 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 Mar 16, 2022 to Mar 23, 2022, covering 25 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).
DREAMTOME 49-30MM/260CM Material Number: M00584010
Boston Scientific Corporation
(1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX component to Liko overhead lift…
Hill-Rom, Inc.
Dreamtome Cannulating Sphincterotome-DREAMTOME 44-20MM/450CM Material Number: M00584060
Boston Scientific Corporation
20544 Vitale Silver calcium Alginate Dressings 4x4, 10/box
CellEra LLC
HYDRATOME RX 49-30MM/260CM Material Number: M00583010
Boston Scientific Corporation
20500 Vitale Silver calcium Alginate Dressing Ropes, 5/box
CellEra LLC
RX CHOLANGIOGRAM KIT - SINGLE Material Number: M00575240 M00575240 M00575280 M00575320 M00575360 M00575380 M00575400 M00575440 M00575480
Boston Scientific Corporation
JAGTOME RX 44-30-260-035 Material Number: M00573060
Boston Scientific Corporation
JAGTOME RX 39-30-450-025 Material Number: M00573110
Boston Scientific Corporation
JAGTOME RX 44-30-450-035 Material Number: M00573070
Boston Scientific Corporation
JAGTOME RX 44-20-450-035 Material Number: M00573050
Boston Scientific Corporation
Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X Fusion Capture reagent-X 4 EA, …
Hologic, Inc
JAGTOME RX 39-30-260-025 Material Number: M00573100
Boston Scientific Corporation
LINQ II Insertable Cardiac Monitor
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
SAFE-T PLUS LUMBARPUNCTURE TRAY ADULT
Bard Peripheral Vascular Inc
ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY
Bard Peripheral Vascular Inc
HYDRATOME RX 44-30MM/450CM Material Number: M00583070
Boston Scientific Corporation
LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP
Bard Peripheral Vascular Inc
BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack
Bio-Rad Laboratories, Inc.
BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL
Bio-Rad Laboratories, Inc.
LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL
Bard Peripheral Vascular Inc
Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer
Bard Peripheral Vascular Inc
20548 Vitale Silver calcium Alginate Dressings 4x8, 5/box
CellEra LLC
JAGTOME RX 39-20-260-025 Material Number: M00573080
Boston Scientific Corporation
JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250
Boston Scientific Corporation
GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated), REF 2082278-001, and MAS700 (Desktop, REF 2082279-001.
GE Healthcare, LLC
DREAMTOME 49-20MM/450CM Material Number: M00584020
Boston Scientific Corporation
Dreamtome RX Cannulating Sphincterotome-DREAMTOME 44-20MM/260CM Material Number: M00584040
Boston Scientific Corporation
STANDARD Q COVID-19 Ag Home Test STANDARD Q COVID-19 Ag Home Test is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV…
SD Biosensor, Inc.
JAGTOME RX 49-30-450-035 Material Number: M00573030
Boston Scientific Corporation
Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC 2.0/2.4 Plate System.
Wright Medical Technology, Inc.
JAGTOME RX 49-30-260-035 Material Number: M00573020
Boston Scientific Corporation
HYDRATOME RX 44-30MM/260CM Material Number: M00583050
Boston Scientific Corporation
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Small Vessel, Catalog number THP-S. For use in peripheral vasculature.
ev3 Inc.
Dispensing Pins for Air Inlet Filter, Product Catalog No. 412005, DP2500 Dispensing Pin W/Valve. A valve for aspiration or injection of medication …
B. Braun Medical, Inc.
VITROS Chemistry Products VersaTips, Catalog No. 6801715 A VersaTip sales unit is composed of 1000 tips per box.
Ortho-Clinical Diagnostics, Inc.
HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Physio-Control, Inc.
Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML or MDS Catalog Number: USA-LP…
Cytocell Ltd.
CoolSeal Generator, REF: CSL-200-50
Bolder Surgical, LLC
PCA 4000 Curing Units, SKU number ACC-06-1000 The PCA 4000 is used for curing industrial resins as well and this recall will not impact units sold…
Envisiontec US Llc
Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
CELLTRION USA INC
Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System products with a Laird chiller WITHOUT an extended drip …
Philips North America Llc
1688 Camera Control Unit (CCU), Catalog number:1688010000. Used in general laparoscopy, nasopharyngoscopy, ear endoscopy, sinuscopy, and plastic sur…
Stryker Corporation
NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip, Ref # 300900 (marketed under EUA202947). Distributed in boxes of 6 assay strips in individual pou…
NeuMoDx Molecular Inc
Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114(Nasal Swab Test)
Lusys Laboratories, Inc.
ExacTrac Dynamic software model numbers: 20910-01, ETD Positioning and Moni. 1.0.0 INST; 20910-01A, ETD Positioning and Moni. 1.0.1 INST; 20910-…
Brainlab AG
Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without an extended drip tray: Model Number: 722031
Philips North America Llc
Thermo Scientific Sensititre Gram Negative Susceptibility Testing Plate, IVD format
Remel Inc
HeartWare Ventricular Assist Device (HVAD) System
Heartware, Inc.
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Multi-vessel, Catalog number THP-M. For use in peripheral vasculature.
ev3 Inc.
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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.