Medical device recalls
Device recalls are the largest single group in this archive, because the FDA logs corrections and removals as well as outright withdrawals. Many are handled entirely between the manufacturer and a hospital and need nothing from a patient. Each notice states who has to act.
13,791 stored notices, reported between Jun 20, 2012 and Oct 28, 2026. Newest first.
Reported Apr 1, 2026
Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Koven Technology, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
FDA (openFDA device enforcement)
Reported Apr 1, 2026
MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2026
CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP15K/B, CENFP17K/A, CENFP19K/A, CENFP23K/A, CENFP27K/A,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Merit Medical Systems, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
High riskUsing this product could cause serious injury, illness or death — stop using it now.Navajo Manufacturing Company
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
10 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthalign, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Philips 3D6-2 Ultrasound Transducer
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Philips Ultrasound, Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Tandem pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tandem Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Diagnostics Scarborough, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Battery Charging Station; Model: 0998-00-0802;
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Datascope Corp.
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Product Description: in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2026
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Artegraft Vascular Graft; REF#: AG740;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LeMaitre Vascular, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Cub Pediatric Crib, Model FL19H
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Mar 18, 2026
Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic streptococcal infection.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Altruan GmbH
2 more products in this recall
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.