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

39,794 recalls · Page 151 of 796

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FDA Medical Devices Recall Insight

According to PlainRecalls' agency ranking (distinct recall events, same sort as /agency), FDA Medical Devices sits #1 of 6 (1st among 6 issuing agencies) with 39,794 notices, about 38.1% of the 104,423-record archive. 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 796 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 5 critical (Class I-equivalent) actions, 45 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 Mar 20, 2024 to Mar 27, 2024, covering 24 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 Mar 27, 2024

MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-775

Angiodynamics, Inc.

Moderate Mar 27, 2024

Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)

D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Moderate Mar 27, 2024

MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-774

Angiodynamics, Inc.

Moderate Mar 27, 2024

MINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-750

Angiodynamics, Inc.

Moderate Mar 27, 2024

Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Mar 27, 2024

TENSIVE Conductive Adhesive Gel, REF 016-401600

Natus Neurology Inc

Critical Mar 27, 2024

HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Sealed Outflow Graft with Bend Relief, Investigational Device Exemption (IDE) 2. HeartMate 3 Sealed Outflow Graft with Bend Relief, US 3. HeartMate 3 Sealed Outflow Graft with Bend Relief, OUS 4. HeartMate 3 LVAS Implant Kit, IDE 5. HeartMate 3 LVAS Implant Kit, US 6. HeartMate 3 LVAS Implant Kit, OUS HeartMate 3 Left Ventricular Assist System: The HeartMate 3 LVAS is designed to provide therapeutic benefit to those affec

Thoratec Corp.

Critical Mar 27, 2024

smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NUS

Smiths Medical ASD Inc.

Moderate Mar 27, 2024

MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756

Angiodynamics, Inc.

Moderate Mar 27, 2024

Medtronic DLP Vessel Cannula, Model Number REF 30000

Medtronic Perfusion Systems

Moderate Mar 27, 2024

MINI STICK MAX 4F X 10 CM STD .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-749

Angiodynamics, Inc.

Critical Mar 27, 2024

HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Sealed Outflow Graft with Bend Relief REF 103393 2. HeartMate II LVAS Implant Kit, US REF 106015 3. HeartMate II LVAS Implant Kit, OUS REF 106016 Update (February 14, 2024) HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II LVAS Implant Kit, OUS REF 102139 2. HeartMate II LVAS Implant Kit, US REF 1355 3. HeartMate II LVAS Implant Kit (with RSOC Controller), US REF 103695 4. HeartMate II LVAS Implant K

Thoratec Corp.

Moderate Mar 27, 2024

Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Mar 27, 2024

I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm,Part Number S65 ST180

In2Bones, SAS

Moderate Mar 27, 2024

impression coping, repositionable, short, screw-retained, PF 4.0

Thommen Medical AG

Moderate Mar 27, 2024

Convatec EsteemBody Soft Convex, Drainable Pouch, Product codes (REF): a) 423643, b) 423658, c) 423659, d) 423664, e) 423666, f) 423645, g) 423667, h) 423657, i) 423652, j) 423646, k) 423654, l) 423653, m) 423647, n) 423644, o) 423648, p) 423665, q) 423656, r) 423651, s) 423660, t) 423661

ConvaTec, Inc

Moderate Mar 27, 2024

MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-752

Angiodynamics, Inc.

Moderate Mar 27, 2024

Access Total T4, REF 33800, IVD, thyroxine reagent assay.

Beckman Coulter, Inc.

Critical Mar 27, 2024

smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS

Smiths Medical ASD Inc.

Moderate Mar 27, 2024

natus neurology, Sleep Supplies Start Kit with Single Use Supplies for Embla EX Series Amplifiers, REF 024252

Natus Neurology Inc

Moderate Mar 27, 2024

microStar Reader, Model Numbers: 10015-000 (marketed in EMEA as 100, 102, 110, and 201), 10016-000 (marketed in EMEA as 101), 10036-000, 10044-000, 10055-000, BC30058, and BC30059

Landauer

Moderate Mar 27, 2024

HDS Traction Boot II, REF AR-6529-23, The Traction Boot is designed to position, support and/or distract the patient's foot for hip surgery

Baxter Healthcare Corporation

Moderate Mar 27, 2024

Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)

D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Moderate Mar 27, 2024

MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-759

Angiodynamics, Inc.

Moderate Mar 27, 2024

Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967

Preat Corp

Moderate Mar 27, 2024

MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-765

Angiodynamics, Inc.

Moderate Mar 27, 2024

Situate Laparotomy Sponge, RF and X-ray Detectable, REF: L1818-04P01C-1

Covidien

Moderate Mar 27, 2024

I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 75mm,Part Number S65 ST175

In2Bones, SAS

Moderate Mar 27, 2024

NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: (1) 48145; (2) 48145E

Mc3 Inc

Moderate Mar 27, 2024

Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023070S

Sarnova HC, Llc

Moderate Mar 27, 2024

MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-751

Angiodynamics, Inc.

Moderate Mar 27, 2024

Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090

Medtronic Inc.

Moderate Mar 27, 2024

MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. - Catalog Number: 45-781

Angiodynamics, Inc.

Moderate Mar 27, 2024

MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-767

Angiodynamics, Inc.

Moderate Mar 27, 2024

Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)

D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Moderate Mar 27, 2024

Abbott Point of Care Control Control i-STAT¿ Level 1 10 X 1.7 mL

Mckesson Medical-Surgical Inc. Corporate Office

Critical Mar 27, 2024

ARROW QuickFlash Radial Artery Catherization (wire, guide, catheter), Part Numbers: a) REF AK-04220; b) REF ASK-04220-FMH1; c) REF ASK-04220-HHC; d) REF ASK-04220-KSP; e) REF ASK-04220-PSU; f) REF ASK-04220-UCL1; g) REF ASK-04500-AH; h) REF ASK-04500-HF-S; i) REF NA-04220-S1A; j) REF NA-04220-X1A; k) REF RA-04220; l) REF RA-04220-W

ARROW INTERNATIONAL Inc.

Moderate Mar 27, 2024

NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: 48135, 48135E

Mc3 Inc

Moderate Mar 27, 2024

MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-758

Angiodynamics, Inc.

Moderate Mar 27, 2024

Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set McKesson Consult" Pregnancy (hCG) Testing Positive Level / Negative Level 2 X 4 mL

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Mar 27, 2024

MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-762

Angiodynamics, Inc.

Moderate Mar 27, 2024

MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-776

Angiodynamics, Inc.

Moderate Mar 27, 2024

Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023060S

Sarnova HC, Llc

Moderate Mar 27, 2024

Liquid Protein Calibrators. C3 and Haptoglobin liquid protein calibrators used with Randox IgA, IgG, and IgM assays that require sample predilution.

Randox Laboratories Ltd.

Moderate Mar 27, 2024

Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System

Think Surgical, Inc.

Moderate Mar 27, 2024

DCA Systems HbA1c Reagent Kit

Siemens Healthcare Diagnostics, Inc.

Moderate Mar 27, 2024

MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 2.75" PG -Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-754

Angiodynamics, Inc.

Moderate Mar 27, 2024

Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL

Mckesson Medical-Surgical Inc. Corporate Office

Moderate Mar 20, 2024

LVP software of the Ivenix Infusion System (IIS), LVP-SW-0004

Fresenius Kabi USA, LLC

Moderate Mar 20, 2024

SPII Model Lubinus, Long Stem Prosthesis XL Neck, cemented

Waldemar Link GmbH & Co. KG (Mfg Site)

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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.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS 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 September 2026.