All recall categories

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.

13,634 stored notices, reported between Jun 20, 2012 and Sep 9, 2026. Newest first.

Medical devices

Reported Apr 15, 2026

NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medline Industries, LP

18 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

See Luer Cap Set, MPC-130, set, administration, intravascular

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Molded Products Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spacelabs Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tornier, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

XTANT Medical Holdings, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Purge Cassette, sold within Impella Pump Sets and Individually Packaged. Labeled and distributed in the below…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Abiomed, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

BD Kiestra" ReadA; Catalog No.: 446948.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bd Kiestra Lab Automation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Burlington Medical, Thyroid Shield.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Burlington Medical, LLC

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardinal Health 200, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Civco Medical Instruments Co. Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

SIGNA Premier systems

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113, 3549313, 354-9314 SILTEX Low Height…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mentor Texas, LP.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Oxoid Australia Pty Limited

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Allura Xper FD10C; System Code: 722001;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems Nederland B.v.

22 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 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)

Medical devices

Reported Apr 8, 2026

Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ReCor Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Reflexion Medical, Inc.

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.