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 225 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 100,165 records spanning 1995 through the present, FDA Medical Devices accounts for roughly 39.0% 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, 47 moderate recalls, and 3 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 20, 2022 to Jul 27, 2022, 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).
LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055
CooperSurgical, Inc.
Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with X-Ray mattress.
Baxter Healthcare Corporation
Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress, REF P3255A01.
Baxter Healthcare Corporation
Ambu VivaSight 2 DLT; endobronchial tube system used for verifying tube placement and repositioning. Catalog numbers 412351000, 412371000, 412391…
Ambu Inc.
BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS)
Becton Dickinson & Company
AESCULAP S4 Cervical Cross Connector L 42-58mm, S4C CROSS CONNECTOR VARIABLE 42-58MM, product code SW117T. Used in spinal fusion surgery.
Aesculap Implant Systems LLC
RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Aesculap Implant Systems LLC
BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)
Becton Dickinson & Company
Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of Erythropoietin concentrations in human s…
R & D Systems, Inc.
Nonsterile convenience kits: (1) regard Item #830099008, CV01005H - CV Part 1 Bundle; and (2) regard Item #830019017, CV00214Q - CV.
ROi CPS LLC
Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Catalog No.383682 (OUS)
Becton Dickinson & Company
AESCULAP S4 Cervical Cross Connector L 33-42mm, S4C CROSS CONNECTOR VARIABLE 33-42MM, product code SW116T. Used in spinal fusion surgery.
Aesculap Implant Systems LLC
AESCULAP S4 Cervical Cross Connector L 28-33mm, S4C CROSS CONNECTOR VARIABLE 28-33MM, SW115T. Used in spinal fusion surgery.
Aesculap Implant Systems LLC
Triton Canister System (finished part numbers FG 12009, for 3L canisters, and FG 12019 for 2L canisters) Scanning Label (component part number 11032)…
Stryker Instruments Div. of Stryker Corporation
BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS)
Becton Dickinson & Company
Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04.
Baxter Healthcare Corporation
Hobbs Medical Polypectomy Snare, Catalog No. 7202
Hobbs Medical, Inc.
RayStation 9B SP1. For radiation treatment planning.
RAYSEARCH LABORATORIES AB
LumiraDx SARS-CoV-2 Antibody (Ab) Test Strip
LumiraDx
BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (OUS)
Becton Dickinson & Company
SX-One MicroKnife
SONEX HEALTH LLC
Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
Aesculap Implant Systems LLC
BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)
Becton Dickinson & Company
BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS)
Becton Dickinson & Company
Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.
ROi CPS LLC
GE Healthcare Avance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009-9050-000; and Aisys CS2 Anesthesia Systems, Part # 1011-9050-000.
GE Healthcare, LLC
Hill-Rom Centrella Pro+ 36" Surface mattress, REF P7923A03.
Baxter Healthcare Corporation
Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6
Stryker Instruments Div. of Stryker Corporation
X80 RADiant Photoelectric Therapy System
Xstrahl Limited
Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.
Baxter Healthcare Corporation
GreenLight HPSEA Laser Fibers, UPN 0010-2092
Boston Scientific Corporation
ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
Aesculap Implant Systems LLC
Hill-Rom PRO+ MRS Surface For Versacare mattress, REF P3255A02.
Baxter Healthcare Corporation
YelloPort Elite Universal Seal. For use in laparoscopic procedures.
Surgical Innovations Ltd
LEFT CORONAL BENDER, TEK1939. Instrument used during spinal surgery.
Aesculap Implant Systems LLC
Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03.
Baxter Healthcare Corporation
Sensis Vibe Combo with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology…
Siemens Medical Solutions USA, Inc
ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
Aesculap Implant Systems LLC
Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK - CE, REF: 91413; TREVO NXT…
Stryker Neurovascular
BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)
Becton Dickinson & Company
Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma. Catalog Number: CH2O0
Randox Laboratories Ltd.
AESCULAP S4 Cervical Cross Connector L22mm, S4C CROSS CONNECTOR FIXED 22MM, product code SW112T. Used in spinal fusion surgery.
Aesculap Implant Systems LLC
AESCULAP S4 Cervical Cross Connector, L26mm, S4C CROSS CONNECTOR FIXED 26MM, product code SW114T. Used in spinal fusion surgery.
Aesculap Implant Systems LLC
Aesculap Sterile disposable fleece drape, Product code: GA414, individually packaged, 50 pieces per shipping unit, product code SZ380R.
Aesculap Implant Systems LLC
Tibial Component Modular. orthopedic prosthesis. Model Nos: Small, W 16-2817/32 Medium, W 16-2817/35 Large,…
Waldemar Link GmbH & Co. KG (Mfg Site)
Ventana HE 600 System, automated slide preparer, for use in laboratories.
Ventana Medical Systems Inc
Wright EVOLVE TRIAD Plate Cutter, REF 49510120
Wright Medical Technology, Inc.
Isopure Sodium Bicarbonate Mixing and Distribution System (IsoMix PRO)
Isopure Corp
DigitalDiagnost 4 High Performance. radiography and fluoroscopy system
Philips Medical Systems DMC GmbH
ProxiDiagnost N90. radiography and fluoroscopy system
Philips Medical Systems DMC GmbH
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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
Read our methodology — how this data is sourced, computed, and verified.