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© 2026Civic Data · Data sourced from OpenFDA, updated weekly · Not affiliated with the U.S. Food and Drug Administration · Always verify against official FDA sources before acting

  1. FDA Recalls
  2. ›Device Recalls

FDA Device Recalls

Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 1–20 of 1,000 recalls

Class IITerminated

Brand Name: Ultra IABP Catheter Kit Product Name: Ultra IABP Catheter Kit Model/Catalog Number: IMU7F-40, IMU7F-35, IMU7F-30, IMU7F-25, and IMU7F-20 Software Version: Not applicable Product Description: The Insightra Ultra IABP Catheter Kit is a 7 French catheter available with either a 40, 35, 30, 25, or 20 cc balloon. The catheter has two lumens and is designed to provide counterpulsation cardiac assist therapy. The outer lumen is a channel for helium used to inflate and deflate the balloon. The inner lumen is used for a guidewire and blood pressure measurement. It is packaged as a convenience kit with accessories (one-way valve, 50 cc syringe, guide wires, introducer needle, dilator, pressure tubing, Datascope & Arrow adaptors). The balloon inflation and deflation cycle is synchronized (using a commercially available control console) with the ECG or arterial pressure to provide counterpulsation synchronized with the heartbeat. It is intended to increase coronary perfusion, decrease the workload of the left ventricle and allow healing of the myocardium Component: No

Insightra Medical Inc

Device contains indications for use and device compatibility claims that have not be reviewed and approved for safety and effectiveness by the FDA. Instructions for use are not consistent with product training.

July 19, 2025 · DeviceView details →
Class IITerminated

BIB Balloon in Balloon Dilatation Catheter. Model Number: 420

Numed Inc

Balloon extension lumens are not printed correctly. Specifically, the inner balloon inflation hub was labeled as the outer balloon, and the outer balloon inflation hub was labeled as the inner balloon.

April 21, 2025 · DeviceView details →
Class IITerminated

CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11

Centers For Disease Control and Prevention

The H5b component may fail to amplify, resulting in an inconclusive result.

April 26, 2024 · DeviceView details →
Class IITerminated

Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25

Vortex Surgical Inc.

Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps Tips occurring in 0.25% of those lots.

December 18, 2023 · DeviceView details →
Class IITerminated

Automated Impella Controller (AIC), product number 0042-040-US with software versions V8.4 and V8.4.1.

Abiomed, Inc.

Pump not detected as connected to controller due to software issue.

October 10, 2023 · DeviceView details →
Class IITerminated

Automated Impella Controller (AIC), product number 0042-000-US with software versions V8.4 and V8.4.1.

Abiomed, Inc.

Pump not detected as connected to controller due to software issue.

October 10, 2023 · DeviceView details →
Class IITerminated

NexGen Precoat Stemmed Tibial Plate Size 5

Zimmer, Inc.

Device outer packaging was incorrectly labeled.

May 19, 2023 · DeviceView details →
Class IITerminated

AVNS ambIT System - PIB/PCA W 2.5in Cath, Product Code: 220509

Avanos Medical, Inc.

Some of the ambIT kits were potentially distributed without an air in-line filter.

April 24, 2023 · DeviceView details →
Class IITerminated

SMMT ambIT Kit Basic Filter Luer Cass, Product Code: 220537

Avanos Medical, Inc.

Some of the ambIT kits were potentially distributed without an air in-line filter.

April 24, 2023 · DeviceView details →
Class IITerminated

ambIT Cassette Filter Male Luer, Product Code: 220266

Avanos Medical, Inc.

Some of the ambIT kits were potentially distributed without an air in-line filter.

April 24, 2023 · DeviceView details →
Class IITerminated

SMMT ambIT Reusable Program - Luer Cass, Product Code: 220568

Avanos Medical, Inc.

Some of the ambIT kits were potentially distributed without an air in-line filter.

April 24, 2023 · DeviceView details →
Class IITerminated

AVNS ambIT System - PIB/PCA W 5in Cath, Product Code: 220507

Avanos Medical, Inc.

Some of the ambIT kits were potentially distributed without an air in-line filter.

April 24, 2023 · DeviceView details →
Class IITerminated

Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one box, and sterile 1 kit consists of 3 pcs. trocar with the valved cannula and 1 pc. infusion cannula.

Mani, Inc. - Kiyohara Facility

A packaging defect may compromise the sterile barrier.

February 20, 2023 · DeviceView details →
Class IITerminated

Sensus Healthcare Inc, SRT-100 Vision IPX 0, HFUS Module IPX 1, with software version 1.9.2; Superficial X-ray Radiation Therapy System with Ultrasonic Imaging Capabilities

Sensus Healthcare, Inc.

When the user pauses the beam delivery, the dose timer is reset (to zero), and as a result may deliver an unexpected dose to the patient.

February 10, 2023 · DeviceView details →
Class IITerminated

Avanos Ballard Oral Care Swab, Bulk Packed, Product Codes: a) 12241, b) 12243, c) 12251

Avanos Medical, Inc.

Incorrect expiration date.

February 3, 2023 · DeviceView details →
Class IITerminated

Mammotome MammoStar Biopsy Site Identified, REF STAR1401

Carbon Medical Technologies, Inc.

The label incorrectly identifies the product as STAR1401, a 1x3mm Barbell shaped marker pre-loaded in a 14 gauge needle, while the packaging contains STAR1402, a 1x5mm Tribell shaped marker pre-loaded in a 14 gauge needle.

December 16, 2022 · DeviceView details →
Class IITerminated

DeRoyal ORGAN RECOVERY PACK PGYBK, a) REF 89-9004.09 and b) 89-9004.10

DeRoyal Industries Inc

DeRoyal is recalling certain lots of surgical procedure pack products that contain a Medtronic Non-Absorbable Suture. The recall is due to Medtronic determining a manufacturing error in the packaging of the non-absorbable sutures that may cause a gap or wrinkle in the breather seal resulting in a sterile barrier breach.

December 12, 2022 · DeviceView details →
Class IITerminated

Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1)

Remington Medical, Inc.

The stylet is longer than specified on the label

December 2, 2022 · DeviceView details →
Class IITerminated

ActiveAid 922, Shower/Commode Chair

Altimate Medical, Inc.

Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position.

November 30, 2022 · DeviceView details →
Class IITerminated

DeRoyal Tonsillectomy Tray, REF 89-10698.01

DeRoyal Industries Inc

DeRoyal is recalling certain lots of surgical procedure pack products that contain a ConMed Foot Controlled Electrosurgical Suction Coagulator. The recall is due to ConMed receiving reports that the suction ports may be occluded on the affected devices. If this occurs, the affected devices will not be able to perform the suction function during use.

November 28, 2022 · DeviceView details →
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