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 13 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 6 critical (Class I-equivalent) actions, 44 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 Jun 10, 2026 to Jun 17, 2026, covering 30 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 17, 2026

MOSAIQ Oncology Information System

Elekta, Inc.

Moderate Jun 17, 2026

Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.45 mm (0.0175 in); REF:TCN-10, TCN Electrode, NITINOL, 10 cm x 0.45 mm (0.0175 in) REF:TCN-15, TCN Electrode, NITINOL, 15 cm x 0.45 mm (0.0175 in); REF:TCN-20, TCN Electrode, NITINOL, 20 cm x 0.45 mm (0.0175 in) REF: TCN-5-3m, TCN Electrode, NITINOL, 3M CABLE, 5 cm x 0.45 mm (0.0175 in) REF: TCN-10-3M, TCN Electrode, NITINOL, 3M CABLE, 10 cm x 0.45 mm (0.0175 in); REF: TCN-15-3M, TCN Electrode, NITINOL, 3M CABL

Boston Scientific Neuromodulation Corporation

Moderate Jun 17, 2026

CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930

INSPIREMD Inc

Moderate Jun 17, 2026

Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay

Siemens Healthcare Diagnostics, Inc.

Moderate Jun 17, 2026

Allia IGS 5 Pulse angiographic X-ray system

GE Medical Systems, LLC

Moderate Jun 17, 2026

Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Model/Catalog Number: 1023770 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 12 bacterial Spore Strips provided by Mesa Labs. The Spore Strip (single species G. stearothermophilus ATCC#7953 or dual species G. stearothermophilus ATCC #7953 and B. atrophaeus ATCC #9372) is intended for use in testing the efficacy of steri

HF Acquisition Co LLC

Moderate Jun 17, 2026

Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316

Avanos Medical, Inc.

Moderate Jun 17, 2026

Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320

Avanos Medical, Inc.

Moderate Jun 17, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No

Avanos Medical, Inc.

Moderate Jun 17, 2026

Plum Duo Precision IV Pump, 40002-0403

ICU Medical, Inc.

Moderate Jun 17, 2026

Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: No

Avanos Medical, Inc.

Moderate Jun 17, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14

Avanos Medical, Inc.

Moderate Jun 17, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20

Avanos Medical, Inc.

Moderate Jun 17, 2026

Halyard, Drape Pack. Kit Code: LMDP36-01.

AVID Medical, Inc.

Moderate Jun 17, 2026

Bicarby" Dialysate; Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G;

Fresenius Medical Care Holdings, Inc.

Moderate Jun 17, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20

Avanos Medical, Inc.

Moderate Jun 17, 2026

DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.

Philips North America Llc

Moderate Jun 17, 2026

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit

Avanos Medical, Inc.

Moderate Jun 17, 2026

Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure.

Boston Scientific Corporation

Moderate Jun 17, 2026

Hintermann Series Talar Implant, Left, Size 2 REF 302112

DT MedTech, LLC

Moderate Jun 17, 2026

Halyard, Eye Bag Pack. Kit Code: UIEB48-01.

AVID Medical, Inc.

Moderate Jun 17, 2026

CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040

INSPIREMD Inc

Moderate Jun 17, 2026

Plum Duo Infusion Pump, 40002-0401

ICU Medical, Inc.

Moderate Jun 17, 2026

Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940

INSPIREMD Inc

Moderate Jun 17, 2026

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

Inter-Med Llc

Moderate Jun 17, 2026

Plum Solo Precision IV Pump, 40001-0401

ICU Medical, Inc.

Moderate Jun 17, 2026

TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201;

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

Moderate Jun 17, 2026

Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation

Medartis AG

Moderate Jun 17, 2026

Allia IGS 7 Pulse angiographic X-ray system

GE Medical Systems, LLC

Moderate Jun 17, 2026

Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software

Abbott Medical

Moderate Jun 17, 2026

EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF: P30P-001x01

BERLIN HEART GMBH

Moderate Jun 17, 2026

CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030

INSPIREMD Inc

Moderate Jun 10, 2026

Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog Number: 555498 Software Version: N/A Product Description: CESK HARRIS METHODIST Component: No

B Braun Medical Inc

Moderate Jun 10, 2026

Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.

Becton Dickinson & Company

Critical Jun 10, 2026

Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211); Spinocan 22 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333231)

B Braun Medical Inc

Moderate Jun 10, 2026

Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050

Covidien LLC

Critical Jun 10, 2026

Atlan A350XL. Model Number: 8621600. anesthesia workstation

Draeger, Inc.

Moderate Jun 10, 2026

Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software Version: N/A Product Description: CESK NORTHSIDE ANESTHESIA TRAY Component: No

B Braun Medical Inc

Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.

Becton Dickinson & Company

Moderate Jun 10, 2026

BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet

CareFusion 303, Inc.

Moderate Jun 10, 2026

Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;

Bayer Medical Care, Inc.

Moderate Jun 10, 2026

Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Moderate Jun 10, 2026

Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product Description: Preface: This report under 21 CFR 806.10 is being submitted for the dV5 system tower, as the NIR Handheld Camera or SOCK is developed and integrated as part of the dV5 system. The affected component of the dV5 system tower is the NIR handheld camera, and is supplied by Schoelly as the manufacturer. Therefore, the product description in this report references t

Intuitive Surgical, Inc.

Moderate Jun 10, 2026

BD Pyxis Mini Main REF: 349 Medication cabinet

CareFusion 303, Inc.

Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.

Becton Dickinson & Company

Moderate Jun 10, 2026

Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E

Kico Knee Innovation Company

Moderate Jun 10, 2026

Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System

Stryker Corporation

Critical Jun 10, 2026

Pediatric care bed; Product Designation: KayserBett IDA;

KAYSERBETTEN GMBH & CO. KG

Moderate Jun 10, 2026

Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4

Daavlin Distributing Company

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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.