-
BD Pyxis: Anesthesia Station ES recall
FDA
· CareFusion 303, Inc. · Class II
-
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm… recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm… recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm… recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus… recall
FDA
· Microbiologics Inc · Class II
-
Proxima Drape labeled as ORTHO TRAUMA CDS, TOTAL KNEE AUX PACK… recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P… recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as HEAD AND NECK OSIS, WILLIS SHOULDER PACK… recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as FACE LIFT. Sterile surgical drape recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as PACK,BASIC,SIRUS,V,5/CS recall
FDA
· Medline Industries, LP · Class II
-
Proxima Drape labeled as DRAPE C-SECTION W/ WINDOW recall
FDA
· Medline Industries, LP · Class II
-
VEIN TRAY, Model No UTVT21C UTVT21C02 UTVT21C-03 recall
FDA
· American Contract Systems Inc · Class II
-
THORACIC PACK , Model No UTTC82Y UTTC82AA-01 recall
FDA
· American Contract Systems Inc · Class II
-
SPINE LUMBAR PACK , Model No UTSL72AA UTSL72AB recall
FDA
· American Contract Systems Inc · Class II
-
OPEN HEART A PACK , Model No UTOH19AI UTOH19AJ-01 UTOH19AJ-02 recall
FDA
· American Contract Systems Inc · Class II
-
MAJOR VASCULAR PACK , Model No UTMV78X-01 UTMV78Y UTMV78Y-01 UTMV78X-01… recall
FDA
· American Contract Systems Inc · Class II
-
GENERAL LAPAROSCOPIC PACK-LF , Model No UTGL53S-06 UTGL53S-07 UTGL53S-08 recall
FDA
· American Contract Systems Inc · Class II
-
AV FISTULA , Model No UTAV77T recall
FDA
· American Contract Systems Inc · Class II
-
NEURO IR TRAY , Model No WENI56J recall
FDA
· American Contract Systems Inc · Class II
-
DIAGNOSTIC NEURO IR TRAY , Model No WENE21 recall
FDA
· American Contract Systems Inc · Class II
-
CV BASIC PUMP PACK , Model No WECV23D recall
FDA
· American Contract Systems Inc · Class II
-
LAPAROSCOPY PACK , Model No SFLA02A SFLA02B recall
FDA
· American Contract Systems Inc · Class II
-
EAR PACK , Model No SFEA12A recall
FDA
· American Contract Systems Inc · Class II
-
LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07B recall
FDA
· American Contract Systems Inc · Class II
-
LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07B recall
FDA
· American Contract Systems Inc · Class II
-
DELIVERY PACK , Model No SGDV22D-01 SGDV22E recall
FDA
· American Contract Systems Inc · Class II
-
TOTAL HIP PACK , Model No SMTH06O SMTH06P recall
FDA
· American Contract Systems Inc · Class II
-
CYSTO , Model No SACY80R recall
FDA
· American Contract Systems Inc · Class II
-
URO ROBOTIC PACK , Model No LVUR44C LVUR44C-03 recall
FDA
· American Contract Systems Inc · Class II
-
LABOR & DELIVERY PPS , Model No LLLD64O LLLD64O-01 LLLD64O-02 recall
FDA
· American Contract Systems Inc · Class II
-
CENTRAL LINE PICC , Model No LLCL44H LLCL44H-01 recall
FDA
· American Contract Systems Inc · Class II
-
C-SECTION PPS , Model No LLCI66M LLCI66M-02 LLCI66M-03 LLCI66M-04 recall
FDA
· American Contract Systems Inc · Class II
-
BORN ON ARRIVAL KIT , Model No LLBN11B recall
FDA
· American Contract Systems Inc · Class II
-
GENERAL ANGIO PACK , Model Nos LLAP75G LLAP75G-01 LLAP75G-02 LLAP75G-03 recall
FDA
· American Contract Systems Inc · Class II
-
OPEN HEART ADULT - SIDE A , Model Nos LLOH01I-01 LLOH01I recall
FDA
· American Contract Systems Inc · Class II
-
LABOR & DELIVERY PACK, Model Nos LLLD19H recall
FDA
· American Contract Systems Inc · Class II
-
LAPAROSCOPY PACK, Model Nos LLLA21J LLLA21J-02 recall
FDA
· American Contract Systems Inc · Class II
-
C-SECTION PACK, Model Nos LLCS44F LLCS44F-01 recall
FDA
· American Contract Systems Inc · Class II
-
CYSTO PACK , Model N. HKCY31A recall
FDA
· American Contract Systems Inc · Class II
-
MAJOR DIEP, Model Nos recall
FDA
· American Contract Systems Inc · Class II
-
HIP SCOPE, Model Nos recall
FDA
· American Contract Systems Inc · Class II
-
DR DIULUS INJECTION PACK, Model Nos recall
FDA
· American Contract Systems Inc · Class II
-
LAPAROSCOPY PACK, Model No recall
FDA
· American Contract Systems Inc · Class II
-
Vista Brite Tip, Judkins Right 4 recall
FDA
· Cordis US Corp · Class II
-
Z1 Femoral Hip System, Product Number 611777612 recall
FDA
· Zimmer, Inc. · Class II
-
Stryker CinchLock Flex Knotless Anchor with Inserter and Suture recall
FDA
· Stryker Corporation · Class II
-
Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors… recall
FDA
· Spectrum Medical Ltd. · Class II
-
DxI 9000 Access Immunoassay Analyzer recall
FDA
· Beckman Coulter, Inc. · Class II
-
Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model recall
FDA
· Intuitive Surgical, Inc. · Class II
-
Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II
-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II
-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II
-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II
-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II
-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II
-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II
-
ZOLL Product Name: Powerheart G5 AED Model recall
FDA
· ZOLL Medical Corporation · Class II