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

39,096 recalls · Page 68 of 782

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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 6 critical (Class I-equivalent) actions, 44 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 49 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 2, 2025 to Apr 9, 2025, covering 20 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 9, 2025

PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP

Ethicon Endo Surgery, LLC

Moderate Apr 9, 2025

PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM

Ethicon Endo Surgery, LLC

Critical Apr 9, 2025

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model/Catalog Number: MP02737 Software Version: Not applicable Pro…

Draeger, Inc.

Moderate Apr 9, 2025

Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S

Stryker Corporation

Moderate Apr 9, 2025

Nasopore 8cm fragmentable nasal dressing, Firm Catalog Number 5400-020-008 and Forte Catalog Number 5400-020-008ITL

Stryker Corporation

Moderate Apr 9, 2025

GE Healthcare Centricity Radiology RA600 (RA600), Model Numbers: 1) 2022296-001; 2) 2033901-001; 3) 2038437-001; 4) 2038437-011; 5) 203843…

GE Healthcare

Moderate Apr 9, 2025

Nasopore Standard 4cm fragmentable nasal dressing, Catalog Numbers 5400-010-004 and 5400-010-004ITL

Stryker Corporation

Moderate Apr 9, 2025

Phoroptor VRx Digital Refraction System Model Numbers: 16242

Reichert, Inc.

Moderate Apr 9, 2025

Boppli: Bedside Device Kit, REF: 54-0002; Sensor Band, REF: 51-0007

PYRAMES INC

Moderate Apr 9, 2025

Nasopore Ex Firm 4cm fragmentable nasal dressing, Catalog Number 5400-030-004 and Nasopore Forte plus 4cm Catalog Number 5400-030-004ITL

Stryker Corporation

Moderate Apr 9, 2025

GE Healthcare Centricity PACS-IW (PACS-IW), Model Numbers: 1) 2042988-001; 2) 2049587-009; 3) 2049587-011; 4) 2049587-012; 5) 2049587-015;…

GE Healthcare

Moderate Apr 9, 2025

Nasopore Ex Firm 8cm fragmentable nasal dressing, Catalog Number 5400-030-008 and Nasopore Forte plus 8cm Catalog Number 5400-030-008ITL

Stryker Corporation

Moderate Apr 9, 2025

Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL

Stryker Corporation

Moderate Apr 9, 2025

Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.

Stryker Spine

Moderate Apr 9, 2025

Pacific Hemostasis Thromboplastin-D, 10 ml. Used in performing one-stage prothrombin time test and factor assays.

Fisher Diagnostics

Moderate Apr 9, 2025

Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754

Terumo Cardiovascular Systems Corporation

Moderate Apr 9, 2025

GE Healthcare Centricity Cardiology CA1000 (CA1000), Model Numbers: 1) 2033901-001; 2) 2038437-001; 3) 2038437-009; 4) 2038437-014; 5) 203…

GE Healthcare

Moderate Apr 9, 2025

Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version: n/a Component: n/a

Qiagen Sciences LLC

Moderate Apr 9, 2025

BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control v…

BD SWITZERLAND SARL

Critical Apr 9, 2025

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable P…

Draeger, Inc.

Moderate Apr 9, 2025

A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.

Medtronic Neuromodulation

Moderate Apr 9, 2025

GE Healthcare Centricity Universal Viewer (UV), Model Numbers: 1) 2066908-077; 2) 2066908-136; 3) 2066908-150; 4) 2088026-003; 5) 2088026-026…

GE Healthcare

Moderate Apr 9, 2025

Otopore Cylinder Standard outer ear dressings, Catalog Numbers 5400-010-000 and 5400-010-000ITL

Stryker Corporation

Moderate Apr 9, 2025

Monterey AL Implant Inserter; 18/20mm; Catalog 48019130.

Stryker Spine

Critical Apr 9, 2025

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Pro…

Draeger, Inc.

Critical Apr 9, 2025

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model/Catalog Number: MP02738 Software Version: Not applicable Pro…

Draeger, Inc.

Critical Apr 9, 2025

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex (P)2 Model/Catalog Number: MP02752 Software Version: Not applicable …

Draeger, Inc.

Moderate Apr 9, 2025

Monterey AL Implant Inserter; 22mm; Catalog 48019140.

Stryker Spine

Moderate Apr 9, 2025

ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH

Ethicon Endo Surgery, LLC

Moderate Apr 9, 2025

Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S

Stryker Corporation

Moderate Apr 9, 2025

DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 The Beckman Coulter DxC 500 A…

Beckman Coulter Inc.

Moderate Apr 9, 2025

PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1

Ethicon Endo Surgery, LLC

Critical Apr 9, 2025

Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Model/Catalog Number: MP01347 Software Version: Not applicable Product Description: Brea…

Draeger, Inc.

Moderate Apr 9, 2025

Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only

Cordis US Corp

Moderate Apr 2, 2025

Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Number 613034700, 2) C SCOPE DISPOSABLE KIT, Pack Number 613034702

MEDLINE INDUSTRIES, LP - Northfield

Moderate Apr 2, 2025

Brand Name: Banner University Med Ctr. Product Name: Cardiac Cath Lab Pack-170278 Model/Catalog Number: GSCC40G Software Version: N/A Product D…

American Contract Systems, Inc.

Moderate Apr 2, 2025

Medline procedure kits labeled as: 1) AV FISTULA PACK-LF, Pack Number DYNJ0826753O; 2) BARRINGTON ACCESSORY TTL KNEE, Pack Number DYNJ56717A; …

MEDLINE INDUSTRIES, LP - Northfield

Moderate Apr 2, 2025

Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS

MEDLINE INDUSTRIES, LP - Northfield

Moderate Apr 2, 2025

Medline procedure kits labeled as: 1) LACERATION TRAY, Pack Number DYNJ17328B

MEDLINE INDUSTRIES, LP - Northfield

Moderate Apr 2, 2025

namic convenience kits labeled as: 1) MTS,4 VALVE,LFT,HRT,KIT-AHS-A*,NW, REF 60010468; 2) MTS,RIGHT HEART,KIT,W/TRANS,ST. *, REF 60010511; 3) …

MEDLINE INDUSTRIES, LP - Northfield

Moderate Apr 2, 2025

Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087

Baxter Healthcare Corporation

Moderate Apr 2, 2025

Baxter Mobile column TruSystem 7500 U, Product Code 1730720

Baxter Healthcare Corporation

Moderate Apr 2, 2025

Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device, sterile, implant grade titanium alloy: (1) REF 82-3300SP, 33mm W x 2…

Orthofix U.S. LLC

Moderate Apr 2, 2025

CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital System Model CM3100 -CardioMEMS Backend Web Application Model CM4000 -M…

St. Jude Medical

Moderate Apr 2, 2025

Baxter TruSystem 7500, Product Code 4091000

Baxter Healthcare Corporation

Moderate Apr 2, 2025

Baxter Stationary column TruSystem 7500, Product Code 1717020

Baxter Healthcare Corporation

Moderate Apr 2, 2025

Medline procedure kits labeled as: 1) ACOUSTIC NEUROMA PACK-LF, Pack Number DYNJ37741B; 2) ANGIOGRAPHY PACK, Pack Number DYNJ21519W; 3) NEURO …

MEDLINE INDUSTRIES, LP - Northfield

Moderate Apr 2, 2025

Prelude IDEAL 4 F Hydrophilic Sheath Introducer, REF: PID4F16021PW/D

Merit Medical Systems, Inc.

Moderate Apr 2, 2025

Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204

Baxter Healthcare Corporation

Moderate Apr 2, 2025

Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086

Baxter Healthcare Corporation

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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.

Compiled from official public sources by the editorial team.

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.