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 61 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 2 critical (Class I-equivalent) actions, 48 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 May 28, 2025 to Jun 4, 2025, covering 14 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 Jun 4, 2025

Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number: 10995498

Siemens Healthcare Diagnostics, Inc.

Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARC CARBON DIOXIDE6X5ML B CALIBRATOR.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

BD MICROBIOLOGY FLUID THIOGLYCOLLATE MED TUBE 1004321196 (100/CT) MEDIA.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

Affinity 4 Birthing Bed, Product Codes P3700E100429, P3700E100432, P3700E100433, P3700E100434, P3700E100435, P3700E100436, P3700E100437, P3700E100438…

Baxter Healthcare Corporation

Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT HBSAG ASSAY(100TST/BX) BDS REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

HEMOCUE INC HEMOTROL LOW 2X1ML LEVEL 1 HEMCUE CONTROL.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumen

Cardinal Health 200, LLC

Moderate Jun 4, 2025

ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376.

Siemens Healthcare Diagnostics, Inc.

Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARC T-UPTAKE ASSAY (100TST/BX) ABBDIA REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

Brand Name: Catalyst+ Product Name: C4D software used in conjunction with Catalyst (SP001-0025), Catalyst HD (SP001-0026), Catalyst PT (S…

C-RAD POSITIONING AB

Moderate Jun 4, 2025

HEMOCUE INC F/GLUCOSE 201 ANALYZER (25/VL 4VL/BX) MICROCUVETTE.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT VITAMIND 6LEVEL CALIBRATOR.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

HEMOCUE INC HEMOTROL HIGH 2X1ML LEVEL 3 HEMCUE CONTROL.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC VITROS PHOSPHORUS (60/CR 5CR/PK) ORCLNL REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

Catalog No. 8888160333; Umbilical Vessel Catheter 3.5 French single lumen

Cardinal Health 200, LLC

Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ALINITY I FREE PSA US(200TEST/EA) REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

GM Helix Acqua Implant, Article Number: 140.984

Straumann USA LLC

Moderate Jun 4, 2025

NxStage PureFlow-B Solution. Catalog numbers: RFP-400, RFP-401, RFP-402, RFP-403, RFP-404, RFP-406, RFP-453, RFP-454, RFP-456.

NxStage Medical Inc

Moderate Jun 4, 2025

Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen

Cardinal Health 200, LLC

Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS PROBE CONDITIONING F/ARCHITECT ANLYZ ABBDIA SOLUTION.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT TOTAL T36X4ML CALIBRATOR.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumen

Cardinal Health 200, LLC

Moderate Jun 4, 2025

ABBOTT RAPID DX N AMERICA LLC CHOLESTECH LDX LIPID PROFILE+GLUCOSE (10/BX 50BX/CS) TEST.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

Catalog No. 8888160556; Umbilical Vessel Catheter 5 French dual lumen

Cardinal Health 200, LLC

Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT HIV COMBO 1X4ML CALIBRATOR.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC VANCOMYCIN (300/BX)ORCLNL REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

ABBOTT RAPID DX N AMERICA LLC HBA1C HEMOGLOBIN AFINION GLYCTD (15TST/BX) TEST KIT.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

ELEOS MALE-FEMALE MIDSECTION 40MM. Part Number: 25001040E. Component of ELEOS Limb Salvage System

Onkos Surgical, Inc.

Moderate Jun 4, 2025

ELEOS COLLAR STEM, CEMENTED, FLUTED, 15MM X 120MM. Model Number: HC-15120-03M. Component of Limb Salvage System with BioGrip.

Onkos Surgical, Inc.

Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC FS(3PK/BX)ORCLNL DILUENT PACK 3.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

ABBOTT RAPID DX N AMERICA LLC MULTI ANALYTE LVL1&2250UL CHOLS CONTROL

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

Plus Initial Drill, Article Number: 103.170;

Straumann USA LLC

Moderate Jun 4, 2025

GM Helix Acqua Implant, Article Number: 140.985

Straumann USA LLC

Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC TOTAL BILI-ALKP XT (L-SEQUESTER) (300/PK) REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

Segmental Stem, Cemented, Bowed, 152MM, 1 EACH. Model Numbers: CB-11152-03M, CB-13152-03M, CB-15152-03M, CB-17152-03M. Component of ELEOS LIMB SAL…

Onkos Surgical, Inc.

Moderate Jun 4, 2025

BD MICROBIOLOGY MAC CONKEY II AGAR (100/CT) 21270 MEDIA.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ALINITY I ANTI-CCPS REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Jun 4, 2025

Male-Female Midsection with the following sizes and model numbers. a. Male-Female Midsection, 40mm, 1 EACH; Model Number: 25001040E b. Male-Fem…

Onkos Surgical, Inc.

Moderate Jun 4, 2025

Segmental Stem, Canal Filling, Bowed 152MM, 1 EACH. Model Numbers: FB-11152-03M, FB-12152-03M, FB-13152-03M, FB-14152-03M, FB-15152-03M, FB-16152-03M…

Onkos Surgical, Inc.

Moderate Jun 4, 2025

ELEOS COLLAR STEM, CEMENTED, FLUTED, 13MM X 120MM. Model Number: HC-13120-03M. Component of Limb Salvage System with BioGrip.

Onkos Surgical, Inc.

Critical May 28, 2025

Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740

C.R. Bard Inc

Moderate May 28, 2025

TRUE 3D VIEWER SYSTEM Model Number EP-00001-XX Software versions 1.0, 1.25, and 1.35 The t3D-Viewer is designed for use by health care professi…

Echopixel, Inc.

Moderate May 28, 2025

Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;

Philips North America Llc

Moderate May 28, 2025

Check=Flo Performer Introducer, 10.0Fr, Reference Part Number(RPN) REF RCFW-10.0-0-38-30-RB, Order Number (GPN) REF G08686,

Cook Incorporated

Moderate May 28, 2025

Product Name: Ingenia 3.0T CX; Model Number: 781271;

Philips North America Llc

Critical May 28, 2025

Centerline Biomedical IOPS Guidewire 2, REF ATW-2; Sensorized wire used to navigate through vasculature to facilitate placement of a catheter

Centerline Biomedical Inc

Moderate May 28, 2025

Product Name: Ingenia 1.5T CX; Model Number: 781262;

Philips North America Llc

Moderate May 28, 2025

Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;

Philips North America Llc

Moderate May 28, 2025

Check=Flo Performer Introducer, 14.0Fr, Reference Part Number(RPN) REF RCFW-14.0-0-38-30-RB, Order Number (GPN) REF G08957,

Cook Incorporated

Moderate May 28, 2025

HiResolution" Bionic Ear System - M Battery Charger Model Number CI-5607

Advanced Bionics, LLC

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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.