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 62 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 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 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 May 21, 2025 to May 28, 2025, covering 21 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).

Critical May 28, 2025

Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300

C.R. Bard Inc

Moderate May 28, 2025

META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690

Smith & Nephew, Inc.

Moderate May 28, 2025

PhenoMATRIX

Copan WASP

Moderate May 28, 2025

Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136;

Philips North America Llc

Moderate May 28, 2025

Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;

Philips North America Llc

Moderate May 28, 2025

Product Name: Ingenia 1.5T S; Model Number: 781347;

Philips North America Llc

Moderate May 28, 2025

Product Name: SmartPath to dStream for 3.0T; Model Number: 782145

Philips North America Llc

Moderate May 28, 2025

Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 782138;

Philips North America Llc

Moderate May 28, 2025

Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137;

Philips North America Llc

Moderate May 28, 2025

Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;

Philips North America Llc

Critical May 28, 2025

Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS

Baxter Healthcare Corporation

Moderate May 28, 2025

Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;

Philips North America Llc

Critical May 28, 2025

Endopath Echelon Vascular White Reload for Advanced Placement Tip (35mm, 4 row); Product code VASECR35

Ethicon Endo-Surgery Inc

Critical May 28, 2025

Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) REF: 0092110

C.R. Bard Inc

Moderate May 28, 2025

Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;

Philips North America Llc

Moderate May 28, 2025

Product Name: SmartPath to dStream for XR and 3.0T; Model Numbers: (1) 781270, (2) 782113;

Philips North America Llc

Moderate May 28, 2025

BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV Catheter 20GX1.00IN STRAIGHT BC, REF: 38…

Becton Dickinson Infusion Therapy Systems, Inc.

Moderate May 28, 2025

Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146

Philips North America Llc

Critical May 28, 2025

Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8" (20.3cm) Balloon X-Ray Opaque R…

C.R. Bard Inc

Critical May 28, 2025

Bard Blakemore Esophageal-Nasogastric Tube (Adult) REF: 0092100

C.R. Bard Inc

Moderate May 28, 2025

Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152;

Philips North America Llc

Moderate May 28, 2025

Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140;

Philips North America Llc

Moderate May 28, 2025

Product Name: Upgrade to MR 7700; Model Number: 782130;

Philips North America Llc

Moderate May 28, 2025

True 3D Viewer, Model: EP-00003

Echopixel, Inc.

Moderate May 21, 2025

Intera 1.5T Master/Nova, Model Number: 781106;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Moderate May 21, 2025

BIB Balloon in Balloon Dilatation Catheter. Model Number: 420

Numed Inc

Moderate May 21, 2025

SmartPath to dStream for 3.0T, Model Number: 782145;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Moderate May 21, 2025

Intera 1.5T Explorer/Nova Dual, Model Number: 781108;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Moderate May 21, 2025

Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395

MEDLINE INDUSTRIES, LP - Northfield

Moderate May 21, 2025

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

Beckman Coulter Inc.

Moderate May 21, 2025

FoundationOne Companion Diagnostic (F1CDx)

Foundation Medicine, Inc.

Moderate May 21, 2025

SmartPath to dStream for 1.5T, Model Number: 782146;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Moderate May 21, 2025

Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit

AVID Medical, Inc.

Moderate May 21, 2025

Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended …

Abbott Molecular, Inc.

Moderate May 21, 2025

Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and other vascular lesions, RPN M…

Cook Incorporated

Moderate May 21, 2025

Intera 1.0T Omni/Stellar, Model Number: 781102;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Moderate May 21, 2025

Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.

AVID Medical, Inc.

Moderate May 21, 2025

Enterprise 1.5T, Model Number: 781145;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Moderate May 21, 2025

PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric s…

Richard Wolf GmbH

Critical May 21, 2025

Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH165 Software Version: N/A Product Description: AirLi…

Vyaire Medical

Moderate May 21, 2025

Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090, a multiplex real-time reverse transcription (RT) polymerase chain reaction…

Abbott Molecular, Inc.

Moderate May 21, 2025

Intera 1.5T Omni/Stellar, Model Number: 781104;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Moderate May 21, 2025

Intera 0.5T Standard, Model Number: 781101;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Moderate May 21, 2025

KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayT…

Klinika Mdical Gmb

Moderate May 21, 2025

Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3012 Product Description: Contour Gold Eyelid Weight, 1.2 gm …

Meddev Corp

Critical May 21, 2025

Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.

Baxter Healthcare Corporation

Moderate May 21, 2025

Intera 3.0T Quasar Dual, Model Number: 781150;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Moderate May 21, 2025

Intera 1.5T Power/Pulsar, Model Number: 781105;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Critical May 21, 2025

iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.

Medical Depot Inc.

Moderate May 21, 2025

Intera 1.5T R11, Model Number: 781170;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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.

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.