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 627 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 1 critical (Class I-equivalent) actions, 46 moderate recalls, and 3 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 15, 2015 to Jul 15, 2015, covering 11 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).
Mississippi Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Arthroscopy Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Philips GoSafe Communicator 7000L Personal emergency response system.
Lifeline Systems, Incorporated
Volcano s5/s5x/CORE Mobile Intravascular Ultrasound Imaging and Pressure System; Product/Part numbers: s5 - 804200-002 and 804200-014; s5x - 807300-…
Volcano Corp
PowerPICC SOLO Catheter with Tip Location System (TLS) Stylet 4F Nurse Full Tray with Microintroducer (with Lidocain) The PowerPICC Solo catheter…
Bard Access Systems
Phleb Pack and Laser Phleb Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
A.L.P.S. Foot Locking Calcaneus Plate,Small-Right. Provides the orthopaedic surgeon a means of bone fixation and helps generally in the management…
Biomet, Inc.
Shoulder Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Endovenous Kit, Endo Pack and Endovenous Laser Kit - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Vasc Custom Kit - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Skin and Vein Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Primus (THE BTE WS30), model PrimusRS (PRRS) and Primus+ (PR30) a measuring exercise equipment device designed to provide active and passive torque r…
BTE Technologies, Inc.
Surgical Pack and General Surgery Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Head & Neck Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Blepharoplasty Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Suction Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
General Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Volcano s5i/s5ix/s5iz/CORE Intravascular Ultrasound Imaging and Pressure System; Product/Part numbers: s5i -806300-020 ; s5ix/s5iz - 807400-001; …
Volcano Corp
Glaucoma Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Knee Arthro Pack and Knee Arthro Pack II - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Pediatric Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Custom Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Vaginal Rejuvenation Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Lipo Pack, Liposuction Expended Pack, and Liposuction Tray - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide Product Usage: The Nakoma-SL ACP System is intended for anterior …
Alliance Partners LLC
The PowerLED / X-TEN / VOLISTA Surgical Light Systems are surgical light systems intended to be used to provide visible illumination of the surgical …
Maquet Cardiovascular Us Sales, Llc
Standard Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Vein & Vascular Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Hand Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
ENT Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
PowerPICC SOLO Catheter with Sherlock 3CG (TPS) Stylet 5F Maximal Barrier Tray with Microintroducer The PowerPICC Solo catheters are intended for…
Bard Access Systems
Plastic Pack and Plastic HNP Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer (Single-Lumen) (Sherlock) The PowerPICC Solo catheters are intended for sh…
Bard Access Systems
Lipo/Buttocks Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Hand Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Vein Pack, Vein Treatment II Pack, Vein Brunswick Pack, Vein No Lidocaine Pack, Vein Ablation Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Face Lift Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Podiatry Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Natrelle Re-sterilizable Breast Implant Sizer, Size: 410 cc, Style No. MSZFX410. The product is packaged in a thermoformed tray (double sterile ba…
Allergan Inc
Face Neck Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Cysto Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Upper Extremity Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Open Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Advanced Vein Care - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
ComboMap Intravascular Flow and Pressure System; Product/Part number: Combo Map - 802745-001. Intravascular Imaging and Pressure System for e…
Volcano Corp
DND Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Tummy Tuck Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
Shiley Neonatal, Pediatric and Long Pediatric Tracheostomy Tube, Cuffless. Model Numbers: 2.5NEF,3.0NEF,3.5NEF,4.0NEF,4.5NEF,2.5PEF,3.0PEF,3.5PEF,4.…
Covidien LP (formerly Nellcor Puritan Bennett Inc.)
Minor Pack and Minor Pack II Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare, LLC.
TITANIUM END CAP WITH T40 STARDRIVE RECESS, 0MM EXTENSION FOR TITANIUM TIBIAL NAILS-EX; Synthes Tibial Nail System EX is intended to stabilize fractu…
Synthes, Inc.
Nearby Agencies
Explore recalls from other federal agencies that share oversight of product safety.
Learn More About Recalls
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
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recall counts and figures reflect FDA Medical Devices's own published filings, aggregated alongside the other two federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.