|
Product Description
|
Recall Class
|
FDA Recall Posting Date
|
Recalling Firm
|
Aveir DR Leadless Pacemaker (LP) Ventricular Device
REF LSP202V
UDI-DI code: 05415067040725
REF...
|
2
|
04/14/2025
|
Abbott Medical
|
Azurion 3 M12, Azurion 3 M15, Allura R9 7 M12, Allura R9 M20, Azurion 7 M12, Azurion 7 M20
The ...
|
2
|
12/18/2017
|
Philips Electronics North America Corporation
|
Bag size #4 Custom Convenience Kits
Usage: Surgical convenience kits
labeled as the followin...
|
2
|
02/27/2019
|
American Contract Systems, Inc.
|
BioEnvelope, surgical mesh envelope. Labeled as the following:
1. BioEnvelope (Medium) (single...
|
2
|
10/04/2019
|
AZIYO BIOLOGICS
|
Boston Scientific Model 3120 ZOOM LATITUDE Programmer/Recorder/Monitor (PRM) installed with Model 28...
|
2
|
01/05/2024
|
Boston Scientific Corporation
|
CONTAK TR (Model no. 1241) pacemaker. Sterilized with gaseous ethylene oxide. Guidant Corporatio...
|
1
|
07/28/2005
|
Guidant Corporation
|
CanGaroo Envelopes labeled as the following:
1. CanGaroo Envelope (Large) (single pack);
2...
|
2
|
10/04/2019
|
AZIYO BIOLOGICS
|
Cardiovascular Allura Centron; Model Number: 722400
The Allura CV2O is intended for physicians (...
|
2
|
01/30/2016
|
Philips Electronics North America Corporation
|
Centron
Product Usage:
Vascular,cardiovascular and neurovascular imaging applications,includin...
|
2
|
07/25/2018
|
Philips Healthcare
|
Centurion procedure kits labeled as:
1) 3" RADIAL ARTERIAL LINE KIT- ICU, Pack Number ART240B;
2)...
|
2
|
08/28/2024
|
MEDLINE INDUSTRIES, LP - Northfield
|