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.

13,791 stored notices, reported between Jun 20, 2012 and Oct 28, 2026. Newest first.

Medical devices

Reported Apr 22, 2026

Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7

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

Insulet Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

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

Integra LifeSciences Corp. (NeuroSciences)

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

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

Linkbio Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F

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

Medline Industries, LP

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Interventional Tool) intended to…

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

Philips Medical Systems Nederland B.v.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Philips Spectral CT on Rails. Model Number: 728334.

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

Philips Medical Systems

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Yeastone Broth, 11ML, 10/BOX YY3462

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

Remel, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

ARTIS Pheno VE30A and VE40A, Model 10849000

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 22, 2026

Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/Catalog Number: CLXUSA Software…

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

Therakos Development Limited

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

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

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

MicroScan Neg MIC 3J REF C54814

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

Beckman Coulter, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

B¿R¿A¿H¿M¿S KRYPTOR compact REACT, REF: 89986, used with B¿R¿A¿H¿M¿S PlGF Plus KRYPTOR, REF: 859075N, and run on the…

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

Brahms GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

COOK MEDICAL Approach CTO-6 Micro Wire Guide, Reference Part Number CMW-14-190-6G, Order Number G50786

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

Cook Incorporated

17 more products in this recall

FDA (openFDA device enforcement)

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)

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Related categories

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.