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 441 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 0 critical (Class I-equivalent) actions, 50 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 40 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 18, 2018 to Jul 18, 2018, covering 19 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).
Femoral Nail, A/R T2 Femur ¿10x320 mm, Product Number 18251032S
Stryker GmbH
BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS (QCV) is an automated test for…
bioMerieux, Inc.
Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S
Stryker GmbH
Femoral Nail, A/R, R1500 T2 Femur ¿12x300 mm, Product Number 18281230S
Stryker GmbH
Percepta CRT-P MRI SureScan, REF W1TR01 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization therapy (…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Percepta Quad CRT-P MRI SureScan, REF W4TR04 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization ther…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems
GE Medical Systems, SCS
Discovery IGS 730 Interventional Fluoroscopic X-ray Systems
GE Medical Systems, SCS
Femoral Nail, A/R, R1500 T2 Femur ¿12x360 mm, Product Number 18281236S
Stryker GmbH
Hyalomatrix, Product nos. 651105, 651103, 651104, and 651301 Product Usage: Hyalomatrix is a bi-layered, sterile, flexible, and comfortable wound…
Anika Therapeutics, Inc.
Peripherally Inserted Midline Catheter Kit with Placement Wire, REF MK-02031-TW Product Usage: To provide real time tip location information of a…
Arrow International Inc
Reliance 1227 Cart and Utensil Washer/Disinfector, FW03101, FW03102, FW03S003 Product Usage: The Reliance 1227 Cart and Utensil Washer/Disinfecto…
Steris Corporation
BARD MYPICC Kit, REF CK000095B, 5F French Size, packaged 5 kits/case, Sterile, RX, For use in vascular access procedures.
Medline Industries, Inc.
VPS TipTracker Stylet Accessory, REF RHY-177-TTSAP Product Usage: To provide real time tip location information of a central venous catheter by u…
Arrow International Inc
Femoral Nail, LEFT T2 GTN ¿14x300 mm, Product Number 18501430S
Stryker GmbH
BCI Advisor Vital Signs Monitor, Model 9200, Reorder numbers 920654235, 920654235, 920654335A, and 920674235A. (The differences in the reorder numbe…
Smiths Medical ASD Inc.
Percepta Quad CRT-P MRI SureScan, REF W4TR01 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization ther…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Femoral Nail, RIGHT T2 GTN ¿14x460 mm, Product Number 18511446S
Stryker GmbH
Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Model # CR2003 Product Usage: The CrAg Lateral Flow Assay is an immunochromatographic test sys…
Immuno-Mycologics, Inc
da Vinci Xi EndoWrist Stapler 45 Reload Green, Model 48445G-03, 12 reloads/box.
Intuitive Surgical, Inc.
Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D153ATG Produ…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
VPS Rhythm ECG Accessory Pack, REF RHY-100-ECGO Product Usage: To provide real time tip location information of a central venous catheter by util…
Arrow International Inc
Ankle Arthrodesis Nail, right T2 Ankle ¿11x300mm, Product Number 18191130S
Stryker GmbH
Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular a…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Femoral Nail, A/R T2 Femur ¿10x340 mm, Product Number 18251034S
Stryker GmbH
Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154VRC Prod…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Femoral Nail, A/R T2 Femur ¿15x240 mm, Product Number 18251524S
Stryker GmbH
Femoral Nail, LEFT T2 GTN ¿10x360 mm, Product Number 18501036S
Stryker GmbH
Femoral Nail, A/R, R1500 T2 Femur ¿10x320 mm, Product Number 18281032S
Stryker GmbH
Femoral Nail, RIGHT T2 GTN ¿9x320 mm, Product Number 18510932S
Stryker GmbH
Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP) Catheter, catalog numbers D135303 and D135304. Product Usage: The Reprocess…
Stryker Sustainability Solutions
Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154ATG Produ…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Discovery IGS 740 Interventional Fluoroscopic X-ray Systems
GE Medical Systems, SCS
PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to determine PD-L1 levels for determination of patient treatment options.
Dako North America Inc.
Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S
Stryker GmbH
BioMerieux mini VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS (QCV) is an automated tes…
bioMerieux, Inc.
Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D153VRC Prod…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Femoral Nail, LEFT T2 GTN ¿12x360 mm, Product Number 18501236S
Stryker GmbH
Femoral Nail, A/R, R1500 T2 Femur ¿12x380 mm, Product Number 18281238S
Stryker GmbH
Proteus 235, Version PTS-11.0.1.2 and PTS-11.0.2 Product Usage: A device designed to produce and deliver a proton beam for the treatment of patie…
Ion Beam Applications S.A.
LigaSure" Exact Dissector Nano Coated 20.6mm-21cm Product Usage: A bipolar electrosurgical instrument intended for use in open surgical procedure…
Covidien LLC
NOVAPLUS(R) Pregnancy Cassette Device with Droppers, Urine hCG Pregnancy Cassette, Cat. No. VPT1-CASS Product Usage: pregnancy test
Ekla Corporation
Percepta CRT-P MRI SureScan, REF W1TR04 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization therapy (…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular a…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Femoral Nail, A/R T2 Femur ¿12x360 mm, Product Number 18251236S
Stryker GmbH
Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU) Product Usage: The vacuum regulator is intended to be used in a medical facilit…
Ohio Medical Corporation
Elecsys Vitamin D total II, Vitamin D Test System, Material number 07464215160 Product Usage: This assay is intended for the quantitative determi…
Roche Diagnostics Corporation
da Vinci Xi EndoWrist Stapler 45 Reload Blue, Model 48645B-03, 12 reloads/box.
Intuitive Surgical, Inc.
Elecsys Vitamin D total II, Vitamin D Test System, Material number 07028148190 Product Usage: This assay is intended for the quantitative determi…
Roche Diagnostics Corporation
AperFix AM Femoral Implant, Model numbers CM-2409 (9mm x 24 mm) and CM-2410 (10 mm x 24 mm). For orthopedic use in ligament reconstruction.
Cayenne Medical Inc.
Nearby Agencies
Explore recalls from other federal agencies that share oversight of product safety.
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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
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.