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  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 301–320 of 1,000 recalls

Class IIITerminated

Neoprobe GDS Control Unit, Model Number NPCU3

Devicor Medical Products Inc

It was discovered during a documentation review that China has the software version as v5.01 approved for use in China. The current software version on devices distributed in China since 2011 is v6.01.

September 7, 2020 · DeviceView details →
Class IIITerminated

Albumin Gen.2, Catalog 05166861190

Roche Diagnostics Operations, Inc.

Roche has confirmed customer complaints of low quality (QC) recovery and invalid calibrations for the identified products. A discoloration (yellow color) was observed and is the result of cross contamination between the R1 and R3 reagents.

August 27, 2020 · DeviceView details →
Class IIITerminated

Tina-quant Complement C4 ver.2, Catalog 05991994190

Roche Diagnostics Operations, Inc.

Roche has confirmed customer complaints of low quality (QC) recovery and invalid calibrations for the identified products. A discoloration (yellow color) was observed and is the result of cross contamination between the R1 and R3 reagents.

August 27, 2020 · DeviceView details →
Class IIITerminated

Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) - Product Usage: Instructions for Use - Centrifugal Pump System is a device that uses a method other than revolving rollers to pump the blood through an extracorporeal circuit Material Number: 701043292

Maquet Cardiovascular Us Sales, Llc

Instruction For Use (IFU) references incorrect serial number of 90437000. It should state This document applies to ROTAFLOW Consoles as of serial number 94175452 affected by the implementation of the new IEC standard 60601 1 2, 4th edition

August 7, 2020 · DeviceView details →
Class IIITerminated

Model No:T-SPOT.TB8, Catalogue No.: TB.300; UDI: 1505171600030 - Product Usage: intended for use as an aid in the diagnosis of Mycobacterium tuberculosis infection by detecting effector T cells that respond to stimulation by M. tuberculosis antigens ESAT-6 and CFP10, and capturing interferon-gamma in the vicinity of these cells.

Oxford Immunotec

Incorrect expiration date included in test kit labeling and/or in Substrate component label.

July 16, 2020 · DeviceView details →
Class IIITerminated

Model No:T-SPOT.TB50, Catalogue No.: TB.50; UDI: 1505171600004 - Product Usage: intended for use as an aid in the diagnosis of Mycobacterium tuberculosis infection by detecting effector T cells that respond to stimulation by M. tuberculosis antigens ESAT-6 and CFP10, and capturing interferon-gamma in the vicinity of these cells.

Oxford Immunotec

Incorrect expiration date included in test kit labeling and/or in Substrate component label.

July 16, 2020 · DeviceView details →
Class IIITerminated

Pointts sistema de ellmlnact!;o de verrugas OTC - Brazil Catalog Number: 1001-0280 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of skin tags.

OraSure Technologies, Inc.

Unit boxes not properly sealed

July 15, 2020 · DeviceView details →
Class IIITerminated

Personelle OTC Skin Tag Remover, Canada Catalog Number: 1001-0314 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of skin tags.

OraSure Technologies, Inc.

Unit boxes not properly sealed

July 15, 2020 · DeviceView details →
Class IIITerminated

CVS Advanced Wart Remover Kit, Catalog Number: 1001-0407 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of common warts and plantar warts.

OraSure Technologies, Inc.

Unit boxes not properly sealed

July 15, 2020 · DeviceView details →
Class IIITerminated

Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 2 plate Matrix Oral Fluid Coated Micro-Plate. IVD Immunoassay for Benzodiazepines, Product Number: 1110IT

OraSure Technologies, Inc.

Incorrect lot number for Standard Oral Fluid Negative Calibrator on specification sheet included in kit and/or additionally same error on unit box

July 13, 2020 · DeviceView details →
Class IIITerminated

Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate Matrix Oral Fluid Coated Micro-Plate-IVD Immunoassay for Benzodiazepines, Product Number: 1110IB

OraSure Technologies, Inc.

Incorrect lot number for Standard Oral Fluid Negative Calibrator on specification sheet included in kit and/or additionally same error on unit box

July 13, 2020 · DeviceView details →
Class IIITerminated

PrepIT Q2A Kit, Model PT-Q2A-96 containing component reagent AG (PT-QAG-96) 1.4mL and ST (PT-QST-96) 2.9mL - Product Usage: used for the removal of SDS and other inhibitors from samples collected using DNA Genotek oral sample collection kits.

DNA Genotek Inc.

Reagents were shipped to customers after the Use by data indicated on its labeling.

June 24, 2020 · DeviceView details →
Class IIITerminated

POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Extended Dwell Catheter made of ChronoFlex C with BioGUARD Technology), Catalog No. 94108, Device UDI 00859821006773/Pacakge UDI 10859821006770 - Product Usage: Introducer with Extended Dwell Catheter is used to gain access to the vascular system to sample blood and administer fluids intravenously. It may also be used for power injection of contrast media up to a rate 8ml/sec, at a maximum of 325 psi fluid pressure.

Access Scientific LLC

Convenience kit mislabeled with the incorrect catheter effective length on the device label and the packaging label. Use may lead to a delay or interruption of treatment and user dissatisfaction or annoyance.

June 15, 2020 · DeviceView details →
Class IIITerminated

Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM handle is the grip for the SLIM driver in orthopedic surgical procedures.

Pega Medical Inc.

The lot number on the pediatric orthopedic implant driver instrument handle does not match the lot number on the label.

April 3, 2020 · DeviceView details →
Class IIIOngoing

ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative software for simulating and evaluating surgical treatment options

Immersivetouch Inc

Observed an internal repetitive software glitch in ImmersiveView.

April 3, 2020 · DeviceView details →
Class IIITerminated

ARCHITECT C Peptide Calibrator - Product Usage: used as an aid in the diagnosis and treatment of patients with abnormal insulin secretion including diabetes mellitus.

Abbott Laboratories

Error in the renewal documentation process for license in Mexico. All in date ARCHITECT C Peptide Reagents, Calibrators and Controls are being recalled until a new license is obtained.

April 1, 2020 · DeviceView details →
Class IIITerminated

ARCHITECT C Peptide Reagent - Product Usage: used as an aid in the diagnosis and treatment of patients with abnormal insulin secretion including diabetes mellitus.

Abbott Laboratories

Error in the renewal documentation process for license in Mexico. All in date ARCHITECT C Peptide Reagents, Calibrators and Controls are being recalled until a new license is obtained.

April 1, 2020 · DeviceView details →
Class IIITerminated

ARCHITECT C Peptide Calibrator - Product Usage: used as an aid in the diagnosis and treatment of patients with abnormal insulin secretion including diabetes mellitus.

Abbott Laboratories

Error in the renewal documentation process for license in Mexico. All in date ARCHITECT C Peptide Reagents, Calibrators and Controls are being recalled until a new license is obtained.

April 1, 2020 · DeviceView details →
Class IIITerminated

Utak NR Trace Elements Serum Control, 5 ml, REF 66816. The responsible firm on the label is UTAK LABORATORIES, INC., Valencia, CA. Control for in vitro diagnostics.

Utak Laboratories Inc

The product has an incorrect reference value for cadmium and an incorrect expected range.

March 20, 2020 · DeviceView details →
Class IIITerminated

VITROS Immunodiagnostic Products TT4 Reagent Pack, Product Code 8744468

Ortho Clinical Diagnostics

The specified reagent packs exhibit an increase in the frequency of unsuccessful calibrations.

March 10, 2020 · DeviceView details →
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