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 237 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 1 critical (Class I-equivalent) actions, 43 moderate recalls, and 6 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 23, 2022 to Apr 6, 2022, covering 24 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).
Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032
Howmedica Osteonics Corp.
Ysiosystem with VC10 software version, Model Number 10281013. Radiographic system
Siemens Medical Solutions USA, Inc
RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5 Service Pack 2 (5.0.2.35), Ray…
RaySearch America Inc
Illumina NextSeq 550Dx, REF: 20005715, CE, IVD
Illumina, Inc.
MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782; …
Medtronic MiniMed
Cytocell 8 Square Template Slides (Glass)- microscope slides Reference: PCN008
Cytocell Ltd.
Compella Therapy Air Supply Unit
Baxter Healthcare Corporation
Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee. The…
Dollar Tree Distribution, Inc.
TCL1 Breakapart Probe, Fluorescence in situ hybridisation (FISH) is a technique allows the visualisation of DNA sequences upon chromosome Catalog N…
Cytocell Ltd.
Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebros…
Integra LifeSciences Corp.
BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE, Item # 856204008. Devices are packaged in a vacuum sealed nylon pouch, which is placed …
Biomet, Inc.
NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects. Catalog Number: 5099250
Ace Surgical Supply Co., Inc.
BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372, 7MM], [Item # 110010373, 8MM], [Item #110018275, 5MM]. De…
Biomet, Inc.
BIOMET TRAUMA Drill Bit, Tap, Guide Pin: [DVR Drill Bit, Item # 212000022, DVR 2.2MM DRILL BIT], [ALPS Drill Bit, Item # 214227160, 2.7X160MM CALIBRA…
Biomet, Inc.
BIOMET Trauma, [Item # 13182-22-26, DVR CROSSLOCK EXTRA LONG PLATE LEFT], [Item # 1318-12-126, DVR CROSSLOCK EXTRA LONG PLATE RIGHT], [Item # 1318-12…
Biomet, Inc.
Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000
Outset Medical, Inc.
Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebros…
Integra LifeSciences Corp.
PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be used to configure customized, tailor-made solutions Catalog Number: 871…
B Braun Medical Inc
Compella Bariatric Bed System
Baxter Healthcare Corporation
Azurion systems with software release R2.0.x
Philips Healthcare
Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators The device is intended to be used in home, institution/hospital, and…
Philips Respironics, Inc.
DigniCap Delta Scalp Cooling System, Product Number: 900-1001, Labeling: The DigniCap Scalp Cooling System User Manual (PN: 0P1DDCD01M-EN_C / IFU 20…
Dignitana, Inc.
HYDRATOME RX 44-20MM/450CM Material Number: M00583060
Boston Scientific Corporation
LYFO Disk
Microbiologics Inc
JAGTOME RX 44-20-260-035 Material Number: M00573040
Boston Scientific Corporation
SAM CHEST SEAL REF CS203-EN Combo LOT Y060321-09
Sam Medical Products
HYDRATOME RX 49-20MM/260CM Material Number: M00583000
Boston Scientific Corporation
DREAMTOME 44-30MM/260CM Material Number: M00584050
Boston Scientific Corporation
Mycoplasma genitalium Control Panel (Inactivated Pellet)
Microbiologics Inc
20545 Vitale Silver calcium Alginate Dressings 4x5, 10/box
CellEra LLC
JAGTOME RX 39-30-260-025 Material Number: M00573100
Boston Scientific Corporation
JAGTOME RX 39-20-450-025 Material Number: M00573090
Boston Scientific Corporation
JAGTOME REVOLUTION RX 39-20-260-025 Material Number: M00584240
Boston Scientific Corporation
LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5
Bard Peripheral Vascular Inc
SAFE-T PLUS ATRAUMATIC ADULT LP TRAY
Bard Peripheral Vascular Inc
Sorin Centrifugal Pump System, CP5, Drive Unit (Catalogue Item #60-01-04, UDI: 04033817900948) used in an HLM S5/C5 System configuration. A cardiopul…
LivaNova Deutschland GmbH
DREAMTOME 49-20MM/260CM Material Number: M00584000
Boston Scientific Corporation
Diagnostic Ultrasound System, ACUSON Juniper, UDI: (01)04056869152059, Model: 11335791, Rx, CE Ultrasound imaging system intended for the follow…
Siemens Medical Solutions USA, Inc.
DREAMTOME 49-30MM/450CM Material Number: M00584030
Boston Scientific Corporation
SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT
Bard Peripheral Vascular Inc
JAGTOME RX 49-20-260-035 Material Number: M00573000
Boston Scientific Corporation
DREAMTOME 44-30MM/450CM Material Number: M00584070
Boston Scientific Corporation
Alinity s System software version2.8.0, REF LN 06P16-01, IVD, OEI: (01)00380740138479 The Alinity s System is intended for In Vitro diagnostic use…
Abbott Laboratories, Inc
JAGTOME REVOLUTION RX 39-30-260-025 Material Number: M00584260
Boston Scientific Corporation
RX CHOLANGIOGRAM KIT Material Numbers: M00575241 M00575281 M00575321 M00575361 M00575381 M00575401 M00575441 M00575481
Boston Scientific Corporation
LUMBAR PUNCTURE DRUG FREE TRAY 22G
Bard Peripheral Vascular Inc
LUMBAR PUNCTURE TRAY ADULT 18G X 3.5
Bard Peripheral Vascular Inc
HYDRATOME RX 44-20MM/260CM Material Number: M00583040
Boston Scientific Corporation
ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G
Bard Peripheral Vascular Inc
20522 Vitale Silver calcium Alginate Dressings 2x2, 10/box
CellEra LLC
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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.