PlainRecalls
2023 data Federal recall API Linked to agency record

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

39,794 recalls · Page 150 of 796

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FDA Medical Devices Recall Insight

According to PlainRecalls' agency ranking (distinct recall events, same sort as /agency), FDA Medical Devices sits #1 of 6 (1st among 6 issuing agencies) with 39,794 notices, about 38.1% of the 104,423-record archive. 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 796 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 10 critical (Class I-equivalent) actions, 40 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).

Moderate Apr 10, 2024

Centurion manual surgical kits labeled as: a) ST. VIRTUS SPLINTER FORCEP 6" (SF8246), Product Code 66580; b) DEBRIDEMENT TRAY, Product Code I86630; c) BIOPSY INSTRUMENT PACK, Product Code I86690; d) DEBRIDEMENT TRAY, Product Code I86815; e) IR ADSON FORCEP & NEEDLE HOLDER, Product Code MNS12675; f) TOENAIL REMOVAL KIT, Product Code SUT20350 MEDLINE GENERAL PURPOSE INST. TRAY, Product Code DYNDA2346A

MEDLINE INDUSTRIES, LP - Northfield

Moderate Apr 10, 2024

Centurion Manual surgical kits labeled as: a) 15ML SAMPLING TUBE WITH CAP, Product Code 15MLVLCP; b) STERILE 9X12 RECLOSABLE BAG, Product Code MG912ST

MEDLINE INDUSTRIES, LP - Northfield

Moderate Apr 10, 2024

Centurion Curette kits labeled as: a) STERILE BUCK EAR CURETTE "00" (25697), Product Code 66745; b) STERILE "1" EAR CURETTE (505629), Product Code 67050; c) STERILE FOX DERMAL CURETTE, 5MM(32923), Product Code 67430; d) STERILE EXCAVATOR CURETTE (P/S), Product Code I67970; e) ST BUCK EAR CURETTE BLNT STR SZ 00, Product Code I68040; f) STERILE BRUNS CURETTE #4 (BC400S), Product Code I68340; g) 6MM FOX DERMAL CURETTE STERILE, Product Code I68380; h) STERILE KEVORKIAN CURETTE 4MM (K

MEDLINE INDUSTRIES, LP - Northfield

Moderate Apr 10, 2024

Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 16o, RIGHT, FOR CEMENTED USE ONLY, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-06-32, b) 41, 44, 47, 50 head, Medium, Item Number314-06-33, c) 44, 47, 50, 53 head, Large, Item Number 314-06-34, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-06-35; Shoulder Arthroplasty

Exactech, Inc.

Moderate Apr 10, 2024

Centurion scalpel handle kits labeled as: a) STERILE # 3 SCALPEL HANDLE, Product Code 66825; b) STERILE PAS #3 BLADE HANDLE (BH3PAS), Product Code I68290

MEDLINE INDUSTRIES, LP - Northfield

Critical Apr 3, 2024

stay-safe /Luer Lock Adapter 4 in

Fresenius Medical Care Holdings, Inc.

Moderate Apr 3, 2024

Bio-Rad, REF: 12005660, QXDx BCR-ABL %IS Kit

Bio-Rad Laboratories

Moderate Apr 3, 2024

Thermalon Stye Compress, Item Number 24352

Bruder Healthcare Company, LLC

Moderate Apr 3, 2024

Baxter Supple Peri-Guard Repair Patch (legacy product codes): a) PC0404SNBIO, b) PC0608NSBIO, c) PC0814SNBIO, d) PC1016SNBIO

Baxter Healthcare Corporation

Moderate Apr 3, 2024

Medivance Neonatal ArcticGel Pads, REF: 31802, 3180202, 31802C

Medivance Inc.

Moderate Apr 3, 2024

IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.

Medical Action Industries, Inc. 306

Critical Apr 3, 2024

stay-safe /Luer Lock Catheter Ext. 18 in

Fresenius Medical Care Holdings, Inc.

Moderate Apr 3, 2024

Epix Universal Clip Applier, REF: CA500, STERILEEO

Applied Medical Resources Corp

Moderate Apr 3, 2024

SYRINGE,BULB,2OZ/60CC,GREEN, Part: 300055070, packaged inside Alcon Custom-Pak Surgical Procedure Packs, Products: 18018-06, 3865-44, 5675-76, 13554-11, 18018-06, 15190-16 , 15190-16, 15190-16, 15190-16, 15190-16, 13554-11, 5918-39, 15190-16, 15190-16, 9208-66, 9208-66, 5675-76, 5918-39, 9208-66, 15190-16, 9065-25, 5918-39, 16066-15, 16066-15

Alcon Research, LLC

Critical Apr 3, 2024

stay-safe /Luer Catheter Ext. 6 in

Fresenius Medical Care Holdings, Inc.

Moderate Apr 3, 2024

RELAY PRO Thoracic Stent-Graft System, containing one endovascular stent-graft system, IFU, and patient tracking card, sterile: (a) Part number 28-M4-34-100-34U; (b) Part number 28-M4-30-095-30U; (c) Part number 28-M4-46-155-46U; (d) Part number 28-M4-32-155-32S; (e) Part number 28-M4-36-250-32S; (f) Part number 28-M4-38-145-34S; (g) Part number 28-M4-38-190-38S; (h) Part number 28-M4-44-105-44S; (i) Part number 28-N4-22-099-22S; (j) Part number 28-N4-22-159-22S; (k) Part number 28-

Bolton Medical Inc.

Moderate Apr 3, 2024

Thermalon Sinus Compress (French), Item Number 24332F

Bruder Healthcare Company, LLC

Moderate Apr 3, 2024

Thermalon Back Wrap, Item Number 24312

Bruder Healthcare Company, LLC

Moderate Apr 3, 2024

Baxter Peri-Guard Repair Patch (new product codes): a) PG0404, b) PG0608, c) PG0814, d) PG1016, e) PG1225

Baxter Healthcare Corporation

Moderate Apr 3, 2024

Thermalon Sinus Compress, Item Number 24332

Bruder Healthcare Company, LLC

Critical Apr 3, 2024

Obsidio Conformable Embolic, Material Numbers (UPN): a) M0013972001010, b) M0013972101010

Boston Scientific Corporation

Moderate Apr 3, 2024

OptiCross Coronary Imaging Catheter, REF H749518080120

Boston Scientific Corporation

Moderate Apr 3, 2024

Insufflation unit, UHI-4.

Olympus Corporation of the Americas

Critical Apr 3, 2024

GeoMed Custom Tracecarts, REF Numbers: a) 53-1831 ORTHO TOTAL JOINT TRACECART, b) 53-1836 GENERAL SURGERY TRACECART

DeRoyal Industries Inc

Moderate Apr 3, 2024

VITROS Performance Verifier I

Ortho-Clinical Diagnostics

Moderate Apr 3, 2024

SOLTIVE Pro SuperPulsed Laser (TFL-SLS )

Olympus Corporation of the Americas

Moderate Apr 3, 2024

Thermalon Neck Wrap, Item Number 24322

Bruder Healthcare Company, LLC

Moderate Apr 3, 2024

InstaClear Lens Cleaner-indicated for use during routine diagnostic procedures and during endoscopic sinus surgery. Model Number: LCS1500UNOL LCS1800UNST LCS4K00UNOL LCS1530BTOL LCS1830BTST LCS4K30BTOL LCS1530TPOL LCS1830TPST LCS4K30TPOL LCS1545BTOL LCS1845BTST LCS4K45BTOL LCS1545TPOL LCS1845TPST LCS4K45TPOL LCS1570BTOL LCS1870BTST LCS4K70BTOL LCS1570TPOL LCS1870TPST LCS4K70TPOL

Olympus Corporation of the Americas

Moderate Apr 3, 2024

Epix Universal Clip Applier, REF: CA500, STERILEEO included within the following kit Reference Numbers: GK1003, AME Kit 54562 GK1004, KIT LAP CHOL DEN HOED 2, GK1005, K2550 - H¿PATECTOMIE ERASME, GK1011, K-19459, GK1014, K-18031 STANDARD KIT, GK1018, K-20735 STANDARD KIT, GK1033, AME STANDARD KIT 21-023, GK1044, KE39830 COLE, GK1047, AME STANDARD KIT 22-003, GK1063, AME STANDARD KIT 22-022, GK1068, AME STANDARD KIT 22-027, GK1071, AME STANDARD KIT 22-030, GK1083, AME STANDARD KIT 22

Applied Medical Resources Corp

Moderate Apr 3, 2024

Access Substrate, REF 81906, For use with the Access Immunoassay Systems

Beckman Coulter, Inc.

Moderate Apr 3, 2024

Baxter Peri-Guard Repair Patch (legacy product codes): a) PC0404NBIO, b) PC0608NBIO, c) PC0814NBIO, d) PC1016NBIO

Baxter Healthcare Corporation

Moderate Apr 3, 2024

SOLTIVE Premium SuperPulsed Laser (TFL-PLS )

Olympus Corporation of the Americas

Moderate Apr 3, 2024

CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X

Philips North America

Moderate Apr 3, 2024

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

Moderate Apr 3, 2024

Cystatin C Calibrator - In vitro diagnostic (IVD) use in the calibration of the Randox Cystatin C assay on automated analysers Catalog Number: CVS 2699

Randox Laboratories Ltd.

Moderate Apr 3, 2024

Baxter Supple Peri-Guard Repair Patch (new product codes): a) SPG0404, b) SPG0406, c) SPG0608, d) SPG0814, e) SPG1016

Baxter Healthcare Corporation

Moderate Apr 3, 2024

O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.

Emergency Products & Research

Moderate Apr 3, 2024

VITROS Performance Verifier II

Ortho-Clinical Diagnostics

Critical Apr 3, 2024

stay-safe /Luer Lock Catheter Ext. 12 in

Fresenius Medical Care Holdings, Inc.

Moderate Apr 3, 2024

Boston Scientific iSLEEVE EXPANDABLE Introducer Set REF H74939349140, facilitates femoral access to the vascular system

Boston Scientific Corporation

Moderate Apr 3, 2024

HydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.

Puritan Medical Products Company, Llc

Critical Apr 3, 2024

stay-safe /Safe Lock Catheter Ext. 12 in

Fresenius Medical Care Holdings, Inc.

Moderate Apr 3, 2024

MediBeads Neck Wrap, Item Number 34320

Bruder Healthcare Company, LLC

Moderate Apr 3, 2024

Thermalon Eye Compress, Item Number 2434

Bruder Healthcare Company, LLC

Moderate Apr 3, 2024

MediBeads King Pad, Item Numbers: 34120, 34120PM, 34125R

Bruder Healthcare Company, LLC

Moderate Apr 3, 2024

Thermalon Heating Pad, Item Number 24002

Bruder Healthcare Company, LLC

Critical Apr 3, 2024

Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); Catalog Number IT1025. Ambulatory Infusion Pump and components

InfuTronix LLC

Critical Apr 3, 2024

Boston Scientific POLARSHEATH Steerable Sheath 12F, REF M004CRBS3050

Boston Scientific Corporation

Critical Apr 3, 2024

Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT1078; Nimbus II EpiD IT1124; Nimbus II EMS IT1063; Ambulatory Infusion Pump and components

InfuTronix LLC

Moderate Apr 3, 2024

Aptima CMV Quant Assay, Reference numbers: AW-22600-001, AW-25509-001, and AW-26381-001 Amplification Reagent, Enzyme Reagent, Promoter Reagent, Amplification Reconstitution Solution, Enzyme Reconstitution Solution, Promoter Reconstruction solution, Target capture Reagent, Reconstitution Collars.

Hologic, 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.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS 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 September 2026.