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 14 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 4 critical (Class I-equivalent) actions, 42 moderate recalls, and 4 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 18, 2026 to Apr 1, 2026, 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).
Pelvic Reconstruction System (PRS) with the below descriptions and corresponding article numbers. 1. Fixation Screw; Article Number: 70312. 2…
I.T.S. GmbH
Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP DRESSING,COLLAGEN,PURACOL PLUS, 2X2.2"
Medline Industries, LP
Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.
Philips Respironics, Inc.
Battery Charging Station; Model: 0998-00-0802;
Datascope Corp.
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
Howmedica Osteonics Corp.
Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell Gamma Knife¿ Elekta Espri…
Elekta, Inc.
Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from va…
GE Medical Systems, LLC
Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Product Description: The STA¿ - Liatest ¿ D-Di kit is …
Diagnostica Stago, Inc.
Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm
ConvaTec, Inc
Convatec, EsteemBody Drainable Pouch REF:423653 10-35mm
ConvaTec, Inc
Artegraft Vascular Graft; REF#: AG740;
LeMaitre Vascular, Inc.
Cub Pediatric Crib, Model FL19H
Stryker Medical Division of Stryker Corporation
Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima HPV assay Component: No
Hologic, Inc.
Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data fro…
GE Medical Systems, LLC
Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description: Influenza A/B virus nu…
Abbott Diagnostics Scarborough, Inc.
Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version …
Baxter Healthcare Corporation
Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from var…
GE Medical Systems, LLC
Convatec, EsteemBody Drainable Pouch REF:423657 10-35mm
ConvaTec, Inc
Endo-Model Replacement Plateau; Item Number: 15-0027/11;
Waldemar Link GmbH & Co. KG (Mfg Site)
Penner Pacific Bathing Spa, Model Numbers 360020-1P
Penner Patient Care, Inc.
GEM Premier 5000 PAK, Part No. 00055360004.
Instrumentation Laboratory
CHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281
Beckman Coulter Mishima K.K.
Owner's Booklets and Instructions for Use that are used with the following blood glucose measurement devices. Description/Item: TRUE METRIX PRO Met…
Trividia Health, Inc.
Artelon FlexBand Dynamic Matrix Ref: 31057
International Life Sciences
GEM Premier 5000; Part No. 00055415005.
Instrumentation Laboratory
Endo-Model Replacement Plateau; Item Number: 15-8030/12;
Waldemar Link GmbH & Co. KG (Mfg Site)
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX…
Trividia Health, Inc.
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
Waldemar Link GmbH & Co. KG (Mfg Site)
Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog Number Z300 UDI-DI code: (01)00628758003007 Raz-ART (Attendant Rotational Tilt) Mobi…
Raz Design Inc
GEM Premier 5000; Model No. 00055430010.
Instrumentation Laboratory
GEM Premier 5000; Part No. 00055430008.
Instrumentation Laboratory
Endo-Model Replacement Plateau; Item Number: 15-8521/15;
Waldemar Link GmbH & Co. KG (Mfg Site)
GEM Premier 5000; Part No. 00055415008.
Instrumentation Laboratory
GEM Premier 5000 PAK; Part No. 00055407511.
Instrumentation Laboratory
Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2) CARDIAC PROCEDURE, Model Num…
Medline Industries, LP
Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05
Exactech, Inc.
Penner Pacific Bathing Spa, Model Numbers 360020-1EP
Penner Patient Care, Inc.
Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 36…
Penner Patient Care, Inc.
GEM Premier 5000 PAK; Part No. 00055360011.
Instrumentation Laboratory
DxC 700 AU, REF: B86444, B86446
Beckman Coulter Mishima K.K.
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902629013 Catalog Number: 11…
Physio-Control, Inc.
Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product De…
Medartis AG
GEM Premier 5000 PAK; Part No. 00055407508.
Instrumentation Laboratory
GEM Premier 5000; Part No. 00055445008.
Instrumentation Laboratory
GEM Premier 5000 PAK; Part No. 00055407510.
Instrumentation Laboratory
GEM Premier 5000 PAK; Part No. 00055360008.
Instrumentation Laboratory
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX…
Trividia Health, Inc.
GEM Premier 5000; Part No. 00055445004.
Instrumentation Laboratory
GEM Premier 5000; Part No. 00055415010.
Instrumentation Laboratory
Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor (Qty 2) 5.0x17mm HEX Anchor (Qty 1) 0.5x12cm FLEXBAND (Qty 1)
International Life Sciences
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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.