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 381 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 0 critical (Class I-equivalent) actions, 50 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 Jul 24, 2019 to Jul 31, 2019, 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 Jul 31, 2019

Merge PACS versions 7.3, 7.3.1, 8.0 and 8.0.1

Merge Healthcare, Inc.

Moderate Jul 31, 2019

Immunoglobulin G is an in vitro diagnostic assay for the quantitative determination of immunoglobulin G in human serum or plasma. Antigen in the sam…

Abbott Laboratories, Inc

Moderate Jul 31, 2019

Artis zee multi, Model Number 10094139

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498

Cardinal Health 200, LLC

Moderate Jul 31, 2019

Apolipoprotein B is an in vitro diagnostic assay for the quantitative determination of apolipoprotein B in human serum or plasma. Antibodies to apol…

Abbott Laboratories, Inc

Moderate Jul 31, 2019

Spacelabs Healthcare Smart Disclosure System, Model 92810, a component of the Intesys Clinical Suite (ICS) G2.

Spacelabs Healthcare, Inc.

Moderate Jul 31, 2019

Terumo Needle, 30G x 1/2", Product Code NN3013R

Terumo Medical Corporation

Moderate Jul 31, 2019

AXIOM Artis TA, Model Number 7007755

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

AXIOM Artis dFC, Model Number 7727717

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

BrightView SPECT, Model Number 882480

Philips Medical Systems (Cleveland) Inc

Moderate Jul 31, 2019

LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120

CooperSurgical, Inc.

Moderate Jul 31, 2019

VITALE Silicon Foam Dressings 4"x4" Cat. No. 20144

CellEra LLC

Moderate Jul 31, 2019

Zyno Medical Administration Set -105"ADMIN SET 20DP W/FILTER 2YSITES CLMP- For Use with Zyno Medical Infusion pumps or Gravity Feed Product Code: …

Zyno Medical LLC

Moderate Jul 31, 2019

Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314

Cardinal Health 200, LLC

Moderate Jul 31, 2019

MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter with add-on check val…

Zevex Incorporated (dba MOOG Medical Devices Group)

Moderate Jul 31, 2019

PulsioFlex Monitoring System, Part Number: 6882747, Model Number: PC400 3 R0. Usage: The PulsioFlex Monitoring System is indicated in patients wh…

GETINGE US SALES LLC

Moderate Jul 31, 2019

BrightView X , Model Number 882478

Philips Medical Systems (Cleveland) Inc

Moderate Jul 31, 2019

AXIOM Artis BA, Model Number 5904656

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363

Cardinal Health 200, LLC

Moderate Jul 31, 2019

RX Daytona, Model Nos. RX4040 and RX4041

Randox Laboratories, Limited

Moderate Jul 31, 2019

Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279

Terumo Medical Corporation

Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548

Cardinal Health 200, LLC

Moderate Jul 31, 2019

Zyno Medical Administration Set -105"ADMIN SET 20DP, W/2 Y SITE, CVCLMPS- For Use with Zyno Medical Infusion pumps or Gravity Feed Product Code:B2…

Zyno Medical LLC

Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 18 G x 1-1/2" Item code: 8881200078

Cardinal Health 200, LLC

Moderate Jul 31, 2019

Terumo Sur-vet Needle, 25G x 5/8", Product Code 100220

Terumo Medical Corporation

Moderate Jul 31, 2019

U3-3 Solar Blue, Laptop integrated power supply used with the Solar Blue Urodynamics for assessing lower urinary tract dysfunctions

LABORIE MEDICAL TECHNOLOGIES, CORP

Moderate Jul 31, 2019

AXIOM Artis BC, Model Number 5904649

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

RX Imola, Model Nos. RX4900

Randox Laboratories, Limited

Moderate Jul 31, 2019

AXIOM Artis FC, Model Number 5904433

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

Transferrin is an in vitro diagnostic assay for the quantitative determination of transferrin in human serum or plasma. Antigen in the sample bond…

Abbott Laboratories, Inc

Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037

Cardinal Health 200, LLC

Moderate Jul 31, 2019

AXIOM Artis dBC, Model Number 5917054

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

AXIOM Artis MP, Model Number 5904466

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer fluids/medication from a container to a patient through a n…

InfuTronix LLC

Moderate Jul 31, 2019

AXIOM Artis TC, Model Number 7728350

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

IGuide System, software versions: 2.2.0, 2.2.1, 2.2.2 Product Usage: Linear Accelerator. The intended use of the device is the control of accur…

Medical Intelligence Medizintechnik Gmbh

Moderate Jul 31, 2019

C3 is an in vitro diagnostic assay for the quantitative determination of C3 in human serum or plasma. Antibodies to C3 combine with C3 in the sample…

Abbott Laboratories, Inc

Moderate Jul 31, 2019

Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654

Cardinal Health 200, LLC

Moderate Jul 31, 2019

The,K -ASSAY HP assay is intended for the quantitative determination of human haptoglobin by immunoturbidimetric assay. The antiserum used in the k…

Abbott Laboratories, Inc

Moderate Jul 31, 2019

AXIOM Artis dFC, Model Number 7412807

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

Artis zee biplane MN, Model Number 10094143

Siemens Medical Solutions USA, Inc

Moderate Jul 31, 2019

Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355

Cardinal Health 200, LLC

Moderate Jul 24, 2019

ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution.

Pharmaceutical Innovations, Inc.

Moderate Jul 24, 2019

Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the UltraDrive System to provide proper irrigation du…

Zimmer Biomet, Inc.

Moderate Jul 24, 2019

Kaluza C Flow Cytometry Software, RX Only in the U.S.A., Beckman Coulter, Inc. for the following software devices: (A) Kaluza C Perpetual License…

Beckman Coulter Inc.

Moderate Jul 24, 2019

Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510

Zimmer Biomet, Inc.

Moderate Jul 24, 2019

The Tina-quant lgA Gen.2 is an immunoturbidimetric assay. Anti-lgA antibodies react with antigen in the sample to form an antigen/antibody complex wh…

Roche Diagnostics Corporation

Moderate Jul 24, 2019

Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage: Electrode Conductivity Spray Solution.

Pharmaceutical Innovations, Inc.

Moderate Jul 24, 2019

A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106)

SpineFrontier, Inc.

Moderate Jul 24, 2019

DeRoyal THE RESOURCE GROUP, CRANI PACK, REF 89-9211.07 custom surgical pack

DeRoyal Industries 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.

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.