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
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).
Merge PACS versions 7.3, 7.3.1, 8.0 and 8.0.1
Merge Healthcare, Inc.
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
Artis zee multi, Model Number 10094139
Siemens Medical Solutions USA, Inc
Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498
Cardinal Health 200, LLC
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
Spacelabs Healthcare Smart Disclosure System, Model 92810, a component of the Intesys Clinical Suite (ICS) G2.
Spacelabs Healthcare, Inc.
Terumo Needle, 30G x 1/2", Product Code NN3013R
Terumo Medical Corporation
AXIOM Artis TA, Model Number 7007755
Siemens Medical Solutions USA, Inc
AXIOM Artis dFC, Model Number 7727717
Siemens Medical Solutions USA, Inc
BrightView SPECT, Model Number 882480
Philips Medical Systems (Cleveland) Inc
LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
CooperSurgical, Inc.
VITALE Silicon Foam Dressings 4"x4" Cat. No. 20144
CellEra LLC
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
Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314
Cardinal Health 200, LLC
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)
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
BrightView X , Model Number 882478
Philips Medical Systems (Cleveland) Inc
AXIOM Artis BA, Model Number 5904656
Siemens Medical Solutions USA, Inc
Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363
Cardinal Health 200, LLC
RX Daytona, Model Nos. RX4040 and RX4041
Randox Laboratories, Limited
Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279
Terumo Medical Corporation
Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548
Cardinal Health 200, LLC
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
Monoject Standard Hypodermic Needle, 18 G x 1-1/2" Item code: 8881200078
Cardinal Health 200, LLC
Terumo Sur-vet Needle, 25G x 5/8", Product Code 100220
Terumo Medical Corporation
U3-3 Solar Blue, Laptop integrated power supply used with the Solar Blue Urodynamics for assessing lower urinary tract dysfunctions
LABORIE MEDICAL TECHNOLOGIES, CORP
AXIOM Artis BC, Model Number 5904649
Siemens Medical Solutions USA, Inc
RX Imola, Model Nos. RX4900
Randox Laboratories, Limited
AXIOM Artis FC, Model Number 5904433
Siemens Medical Solutions USA, Inc
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
Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037
Cardinal Health 200, LLC
AXIOM Artis dBC, Model Number 5917054
Siemens Medical Solutions USA, Inc
AXIOM Artis MP, Model Number 5904466
Siemens Medical Solutions USA, Inc
Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer fluids/medication from a container to a patient through a n…
InfuTronix LLC
AXIOM Artis TC, Model Number 7728350
Siemens Medical Solutions USA, Inc
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
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
Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654
Cardinal Health 200, LLC
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
AXIOM Artis dFC, Model Number 7412807
Siemens Medical Solutions USA, Inc
Artis zee biplane MN, Model Number 10094143
Siemens Medical Solutions USA, Inc
Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355
Cardinal Health 200, LLC
ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution.
Pharmaceutical Innovations, Inc.
Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the UltraDrive System to provide proper irrigation du…
Zimmer Biomet, Inc.
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.
Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510
Zimmer Biomet, Inc.
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
Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage: Electrode Conductivity Spray Solution.
Pharmaceutical Innovations, Inc.
A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106)
SpineFrontier, Inc.
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.
- Source: FDA Medical Devices - verify with the issuing agency: official recall page →
- Source: PlainRecalls Data Index - aggregated from FDA openFDA, CPSC, and NHTSA public databases
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.