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 244 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 1 critical (Class I-equivalent) actions, 47 moderate recalls, and 2 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 Jan 5, 2022 to Jan 19, 2022, covering 27 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).
Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S080032
PTW NORTH AMERICA CORPORATION
LigaSure Blunt Tip Laparoscopic Sealer/Divider, Nano-Coated, Product Number LF1837
Covidien Llc
RefleXion Medical Radiotherapy System - System Label: "*** refleXion REF RXM1000 ***" Physics Guide/Treatment Delivery User Manual/Treatment P…
Reflexion Medical, Inc.
Vaporizer Sevoflurane Maquet Filling, Part No. 6886601 Component of the following systems: Product Code(s) UPN/UDI: Flow-c Anesthesia System 68…
Getinge Usa Sales Inc
OCT-Camera 211 01 A1, Running software iOCT-Control 3 v1.4
Haag-Streit USA Inc
GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600
DePuy Orthopaedics, Inc.
Wireless Footswtich used with the following Philips Allura Xper and Azurion Interventional Fluoroscopic X-ray System . Model Number: 722001, 722002,…
Philips North America Llc
GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100
DePuy Orthopaedics, Inc.
Ki Mobility, Little Wave Tyke (Weight Limit: 95 lbs), Specifically the IFU The Little Wave Tyke is a manually operated device that can be used for m…
Ki Mobility Llc
GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610
DePuy Orthopaedics, Inc.
GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100
DePuy Orthopaedics, Inc.
QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA EUA 200075); REF 691223
Qiagen Sciences LLC
Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: IFX-20R, IFX-20SP, IF…
Invacare Corporation
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Medshape, INC.
DBB-06 Hemodialysis Delivery System
Nikkiso Ltd - Shizuoka Plant
UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.
Uromedica Inc.
Triathlon Pro Tibial Preparation Tray, Revision AC- for organization, storage, and transport in preparation for sterilization of re-usable instrument…
Howmedica Osteonics Corp.
Biomeme SARS-CoV-2- Real Time RT-PCR Test, Instructions for Use, Part number 100002824 Subcomponent of: SARS-CoV-2 Go-Strips, 3000555; SARS-CoV-2 Go…
Biomeme, Inc.
Alinity m System, Part No. 08N53-002
Abbott Molecular, Inc.
iontoPATCH On-the-Go Patch Therapy, Transdermal Iontophoretic Drug Delivery System, Extra Strength, 8-HOUR Average Wear Time, 6/1-patch pouches/box.…
Tapemark Company
Alinity m System, Part No. 08N53-002
Abbott Molecular, Inc.
Alinity m System, Part No. 08N53-002
Abbott Molecular, Inc.
Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: TDX SP2: TDXSP2, TDXSP2…
Invacare Corporation
Alinity m System, Part No. 08N53-002
Abbott Molecular, Inc.
Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: SRX-20R, SRX-20S…
Invacare Corporation
Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue Ratchet Handle in order to fac…
Flower Orthopedics Corporation
Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An automated, clinical chemistry analyzer designed to perform in vitro diagnostic …
Siemens Healthcare Diagnostics, Inc.
Instructions for Use for all model numbers of the Medtronic Abre Venous Self-Expanding Stent System.
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455
DiaSorin Molecular LLC
iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States); iDesign Refractive Studio Aberromete…
AMO Manufacturing USA, LLC
ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray photon and electron radiation for the therapeutic treatment of cancer. M…
Siemens Medical Solutions USA, Inc
VIDAS RUB IgG (RBG), REF 30226
bioMerieux, Inc.
VIDAS FSH, REF 30407-01
bioMerieux, Inc.
Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM
Abbott
VIDAS SARS-COV-2 IgM, Ref 423833-01
bioMerieux, Inc.
VIDAS TOXO IgG Avidity (TXGA), REF 30222-01
bioMerieux, Inc.
Affected components are limited to the Monoprice charging cable (Product # 4867) and 24W iClever Boost Cube charging brick components for the SoundPO…
Forbes Rehab Services Inc
VIDAS Estradiol II, REF 30431-01
bioMerieux, Inc.
Atellica CH ¿2-Microglobulin (B2M) -M) Assay for in vitro diagnostic use in the quantitative determination of ¿2-microglobulin in human serum and pla…
Siemens Healthcare Diagnostics, Inc.
VIDAS Lyme IgG II (LYM), REF 417401
bioMerieux, Inc.
Catalys Precision Laser System, Models: Catalys-U (United States), Catalys-I (International), Catalys-C (China); and Catalys Precision Laser System N…
AMO Manufacturing USA, LLC
VIDAS PRG Progesterone, REF 30409-01
bioMerieux, Inc.
VIDAS LH, REF 30406-01
bioMerieux, Inc.
VIDAS Measles IgG (MSG), REF 30219
bioMerieux, Inc.
VIDAS Clostridium Difficile GDH, REF 30125-01
bioMerieux, Inc.
VIDAS DEX@, Dimer Exclusion II, REF 30455-01
bioMerieux, Inc.
VIDAS Lyme IgM II (LYM), REF 416436
bioMerieux, Inc.
VIDAS B.R.A.H.M.S. PROCALCITONIN PCT, REF 30450-01
bioMerieux, Inc.
VIDAS Mumps IgG (MPG), REF 30218
bioMerieux, Inc.
RAPID 20 E, REF 20701, System for the identification of Enterobacteriaceae in 4 hours, 25 strips/package, IVD.
Biomerieux 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
Read our methodology — how this data is sourced, computed, and verified.