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 176 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 34 critical (Class I-equivalent) actions, 15 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 Jul 5, 2023 to Jul 12, 2023, covering 14 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).
Beside panel FRU (Field Replacement Units) Kits
DATEX--OHMEDA, INC.
TruSignal Wrap Sensor, REF TS-W-D; Oximeter
GE Healthcare Finland Oy
TRACKMASTER, TREADMILL GE T2100-ST2 220V, MODEL NUMBER 317-07927GE
Full Vision Inc
TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-N; Oximeter
GE Healthcare Finland Oy
TruSignal Integrated Ear Sensor with GE Connector REF TS-E2-GE; Oximeter, Ear
GE Healthcare Finland Oy
TissueMend; Advanced Soft Tissue Repair Matrix; Rx Only; Sizes 5x6 cm, 6x10 cm, and 3x3 cm.
TEI Biosciences, Inc.
Giraffe OmniBed, with the following Model Numbers: 6650-0004-901, 6650-0001-901, 6650-0003-901, 6650-0002-901, 6650-0094-901, 6650-0001-9901, 6650-00…
DATEX--OHMEDA, INC.
TruSignal Ear Sensor, REF TS-E-D; Oximeter
GE Healthcare Finland Oy
TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE
Full Vision Inc
TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927
Full Vision Inc
SurgiMend PRS; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x15 cm Semi-Oval, 7x17 cm Fenestrated, 10x20 cm Fenestrated, 8x16 cm …
TEI Biosciences, Inc.
TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928
Full Vision Inc
BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or…
T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.
LinkSymphoKnee Distal Femoral Augment - Tilastan - Size 7-8, Medial-Right/Lateral Left, 5mm- Intended for primary and revision total knee replacement…
Waldemar Link GmbH & Co. KG (Mfg Site)
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085
TELEFLEX LLC
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035
TELEFLEX LLC
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055
TELEFLEX LLC
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082075
TELEFLEX LLC
MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during electrosurgery
Megadyne Medical Products, Inc.
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150055
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181055
TELEFLEX LLC
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090
TELEFLEX LLC
Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380065
TELEFLEX LLC
Integre Pro Yellow LP561, Integre Pro Yellow LP6RY, Integre Pro Scan Green LP6G, Integre Pro Green LP5532 Spare, Optics Bench V2, L2G/LP6G
Ellex Medical Pty Ltd.
RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480030
TELEFLEX LLC
Immunoassay Premium Level 3-In vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes. Ca…
Randox Laboratories Ltd.
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180070
TELEFLEX LLC
Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380050
TELEFLEX LLC
Design Options¿ / Epidural anesthesia kit (10 count carton)
B. Braun Medical, Inc.
PushTracker E2 component utilized with the SmartDrive MX2+ Power Assist Device (Part Numbers: MX2-32K, MX2-32P, MX2-32PK, MX2-33D, MX2-33P, MX2-33PK…
Permobil
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780085
TELEFLEX LLC
Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380030
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170140
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780060
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150025
TELEFLEX LLC
MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during electrosurgery
Megadyne Medical Products, Inc.
Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Medium (Agar)(100mm), 10/pk, REF 01503. For In Vitro Dia…
Remel, Inc
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181045
TELEFLEX LLC
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080100
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170090
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780075
TELEFLEX LLC
Philips Respironics V60 Ventilator-Intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in…
DRE Medical Group Inc
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170065
TELEFLEX LLC
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180050
TELEFLEX LLC
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082060
TELEFLEX LLC
MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery
Megadyne Medical Products, 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.