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 136 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 9 critical (Class I-equivalent) actions, 41 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 Apr 3, 2024 to Apr 10, 2024, covering 22 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).
BD Phoenix NMIC-306 Panel is a self-inoculating (when used with a BD Phoenix Automated Microbiology System) polystyrene panel (tray) containing contr…
Becton Dickinson & Co.
Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 16o, LEFT, FOR CEMENTED USE ONLY, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-…
Exactech, Inc.
Centurion manual surgical kits labeled as: a) ST. VIRTUS SPLINTER FORCEP 6" (SF8246), Product Code 66580; b) DEBRIDEMENT TRAY, Product Code I8663…
MEDLINE INDUSTRIES, LP - Northfield
Centurion Manual surgical kits labeled as: a) 15ML SAMPLING TUBE WITH CAP, Product Code 15MLVLCP; b) STERILE 9X12 RECLOSABLE BAG, Product Code M…
MEDLINE INDUSTRIES, LP - Northfield
Centurion Curette kits labeled as: a) STERILE BUCK EAR CURETTE "00" (25697), Product Code 66745; b) STERILE "1" EAR CURETTE (505629), Product Cod…
MEDLINE INDUSTRIES, LP - Northfield
Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 16o, RIGHT, FOR CEMENTED USE ONLY, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314…
Exactech, Inc.
Centurion scalpel handle kits labeled as: a) STERILE # 3 SCALPEL HANDLE, Product Code 66825; b) STERILE PAS #3 BLADE HANDLE (BH3PAS), Product Code…
MEDLINE INDUSTRIES, LP - Northfield
stay-safe /Luer Lock Adapter 4 in
Fresenius Medical Care Holdings, Inc.
Bio-Rad, REF: 12005660, QXDx BCR-ABL %IS Kit
Bio-Rad Laboratories
Thermalon Stye Compress, Item Number 24352
Bruder Healthcare Company, LLC
Baxter Supple Peri-Guard Repair Patch (legacy product codes): a) PC0404SNBIO, b) PC0608NSBIO, c) PC0814SNBIO, d) PC1016SNBIO
Baxter Healthcare Corporation
Medivance Neonatal ArcticGel Pads, REF: 31802, 3180202, 31802C
Medivance Inc.
IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.
Medical Action Industries, Inc. 306
stay-safe /Luer Lock Catheter Ext. 18 in
Fresenius Medical Care Holdings, Inc.
Epix Universal Clip Applier, REF: CA500, STERILEEO
Applied Medical Resources Corp
SYRINGE,BULB,2OZ/60CC,GREEN, Part: 300055070, packaged inside Alcon Custom-Pak Surgical Procedure Packs, Products: 18018-06, 3865-44, 5675-76, 13554…
Alcon Research, LLC
stay-safe /Luer Catheter Ext. 6 in
Fresenius Medical Care Holdings, Inc.
RELAY PRO Thoracic Stent-Graft System, containing one endovascular stent-graft system, IFU, and patient tracking card, sterile: (a) Part number 28…
Bolton Medical Inc.
Thermalon Sinus Compress (French), Item Number 24332F
Bruder Healthcare Company, LLC
Thermalon Back Wrap, Item Number 24312
Bruder Healthcare Company, LLC
Baxter Peri-Guard Repair Patch (new product codes): a) PG0404, b) PG0608, c) PG0814, d) PG1016, e) PG1225
Baxter Healthcare Corporation
Thermalon Sinus Compress, Item Number 24332
Bruder Healthcare Company, LLC
Obsidio Conformable Embolic, Material Numbers (UPN): a) M0013972001010, b) M0013972101010
Boston Scientific Corporation
OptiCross Coronary Imaging Catheter, REF H749518080120
Boston Scientific Corporation
Insufflation unit, UHI-4.
Olympus Corporation of the Americas
GeoMed Custom Tracecarts, REF Numbers: a) 53-1831 ORTHO TOTAL JOINT TRACECART, b) 53-1836 GENERAL SURGERY TRACECART
DeRoyal Industries Inc
VITROS Performance Verifier I
Ortho-Clinical Diagnostics
SOLTIVE Pro SuperPulsed Laser (TFL-SLS )
Olympus Corporation of the Americas
Thermalon Neck Wrap, Item Number 24322
Bruder Healthcare Company, LLC
InstaClear Lens Cleaner-indicated for use during routine diagnostic procedures and during endoscopic sinus surgery. Model Number: LCS1500UNOL LCS1…
Olympus Corporation of the Americas
Epix Universal Clip Applier, REF: CA500, STERILEEO included within the following kit Reference Numbers: GK1003, AME Kit 54562 GK1004, KIT LAP CHOL …
Applied Medical Resources Corp
Access Substrate, REF 81906, For use with the Access Immunoassay Systems
Beckman Coulter, Inc.
Baxter Peri-Guard Repair Patch (legacy product codes): a) PC0404NBIO, b) PC0608NBIO, c) PC0814NBIO, d) PC1016NBIO
Baxter Healthcare Corporation
SOLTIVE Premium SuperPulsed Laser (TFL-PLS )
Olympus Corporation of the Americas
CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
Philips North America
Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version Number 4.X
Philips North America
Cystatin C Calibrator - In vitro diagnostic (IVD) use in the calibration of the Randox Cystatin C assay on automated analysers Catalog Number: CVS 2…
Randox Laboratories Ltd.
Baxter Supple Peri-Guard Repair Patch (new product codes): a) SPG0404, b) SPG0406, c) SPG0608, d) SPG0814, e) SPG1016
Baxter Healthcare Corporation
O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
Emergency Products & Research
VITROS Performance Verifier II
Ortho-Clinical Diagnostics
stay-safe /Luer Lock Catheter Ext. 12 in
Fresenius Medical Care Holdings, Inc.
Boston Scientific iSLEEVE EXPANDABLE Introducer Set REF H74939349140, facilitates femoral access to the vascular system
Boston Scientific Corporation
HydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.
Puritan Medical Products Company, Llc
stay-safe /Safe Lock Catheter Ext. 12 in
Fresenius Medical Care Holdings, Inc.
MediBeads Neck Wrap, Item Number 34320
Bruder Healthcare Company, LLC
Thermalon Eye Compress, Item Number 2434
Bruder Healthcare Company, LLC
MediBeads King Pad, Item Numbers: 34120, 34120PM, 34125R
Bruder Healthcare Company, LLC
Thermalon Heating Pad, Item Number 24002
Bruder Healthcare Company, LLC
Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); Catalog Number IT1025. Ambulatory Infusion Pump…
InfuTronix LLC
Boston Scientific POLARSHEATH Steerable Sheath 12F, REF M004CRBS3050
Boston Scientific Corporation
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
Read our methodology — how this data is sourced, computed, and verified.