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 178 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 38 critical (Class I-equivalent) actions, 12 moderate recalls, and 0 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 5, 2023, covering 12 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).
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781070
TELEFLEX LLC
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504555
TELEFLEX LLC
MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during electrosurgery
Megadyne Medical Products, Inc.
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080065
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780045
TELEFLEX LLC
LEGACY SMARTBASE, NE 3.0D 1MML, REF: 8730-81NE; LEGACY SMARTBASE, NE 3.0D 2MML, REF 8730-82NE; LEGACY SMARTBASE NARROW NE 3.5D, REF: 8735-80NNE; L…
Implant Direct Sybron Manufacturing LLC
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504580
TELEFLEX LLC
Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506530
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170125
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150040
TELEFLEX LLC
MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used during electrosurgery
Megadyne Medical Products, Inc.
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060
TELEFLEX LLC
DigitalDiagnost C90, Model No. 712034 and 712035
Philips North America Llc
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504590
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180040
TELEFLEX LLC
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504550
TELEFLEX LLC
Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380045
TELEFLEX LLC
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045
TELEFLEX LLC
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382050
TELEFLEX LLC
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082085
TELEFLEX LLC
RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040
TELEFLEX LLC
Sertera 14 Gauge Biopsy Device-intended to obtain percutaneous core biopsy samples from soft tissue and tumors of the breast REF: SERTERA-14
Hologic, Inc
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170055
TELEFLEX LLC
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left
Waldemar Link GmbH & Co. KG (Mfg Site)
RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.
Appliedvr
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135
TELEFLEX LLC
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504575
TELEFLEX LLC
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181065
TELEFLEX LLC
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080070
TELEFLEX LLC
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080090
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780070
TELEFLEX LLC
REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R
Limacorporate S.p.A
Access Hybritech p2PSA reagent, REF B03704 and REF A49752.
Beckman Coulter, Inc.
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080085
TELEFLEX LLC
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Right
Waldemar Link GmbH & Co. KG (Mfg Site)
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504565
TELEFLEX LLC
wDR 2.2 Mobile Digital Diagnostic X-Ray System
SEDECAL SA
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082055
TELEFLEX LLC
MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during electrosurgery
Megadyne Medical Products, Inc.
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170070
TELEFLEX LLC
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right
Waldemar Link GmbH & Co. KG (Mfg Site)
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150035
TELEFLEX LLC
Verigene Enteric Pathogens Nucleic Acid Test (EP), REF 30-002-023
Luminex Corporation
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180030
TELEFLEX LLC
Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506525
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035
TELEFLEX LLC
Perifix¿ / Epidural anesthesia kit (10 count carton)
B. Braun Medical, 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.