173 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Terminated
×
Various Types, Sterile/Nonsterile Stainless Steel Nonabsorable Surgical Sutures-SS Wire, STL MF 7 HSCX48 1N 18 X2, Catalog #29-6567M2; SS Wire, STL MF 6 HSCX48 1N 18 X6, Catalog #29-6619M6, SS Wire, STL MF 6 K-60 1N 18"X8, Catalog #29-7270M8,SS Wire, STL MF 5 K-60/ B-60 1N18 X7, Catalog #29-9001M7, SS Wire, STL MF 5 K-61 1N 2X30, Catalog # E2-5367M2, SS Wire, STL MF 5 K-60 1N 6X18, Catalog # E29-5652M6, SS Wire, STL MF 6 K-60 1N 4X18, Catalog # E29-7270M4,SS Wire, STL MF 5 K-60 1N 45CM, Catalog # E29-7272B, SS Wire, STL MF 5 K-60 2N 30, Catalog #X-2235, SS Wire, STL MF 0 KC-6 1N 18, Catalog #X-3399.
FDA Recall
Terminated
·Product code GAM·June 6, 2007
Neos Vanadium Excavator Part Number 591/0 SCHE
FDA Recall
Terminated
·Sybron Dental Specialties·Product code EKC·November 14, 2008
MicroTox (AMT Item Number/ AMT Description): MTPA-6MBAU / "MicroTox (AMP300/BZO200)+(COC300/THC50)+ (MET300/MOR300) With Cr, Ni, pH, Bl, S.G.", MTPA-6MBAU/ "MicroTox (AMP300/BZO200)+(COC300/THC50)+ (MET300/MOR300) With Cr, Ni, pH, Bl, S.G."
FDA Recall
Terminated
·Ameditech Inc·Product code DKC·August 18, 2020
ImmuTest Drugs of Abuse Cup (AMT Item Number/ AMT Description): IMCA-5AB-W / "ImmuTest Drugs of Abuse Cup AMP1000+BZO300+COC300+OPI2000+THC50 With Cr, Ni, pH, Bl, S.G.", IMC-8BBCE/ "ImmuTest Drugs of Abuse Cup 8 Drug Detection: (COC300/THC50)+AMP1000+BZO300+BUP10+MET500+MTD300+OPI300 NO ADULTERATION", IMCA-8CM5 /"ImmuTest Drugs of Abuse Cup (OXY100/MDMA500)+(PCP25/AMP1000)+COC150+MET500+OPI2000+THC50 with Cr, Ni, pH, Bl, S.G."
FDA Recall
Terminated
·Ameditech Inc·Product code DKC·August 18, 2020
MicroScreen (AMT Item Number/ AMT Description): MSCA-6MBAU/ "MicroScreen AMP300/BZO200/COC300/MET300/OPI300/ THC50 with Cr, Ni, pH, Bl, S.G. "
FDA Recall
Terminated
·Ameditech Inc·Product code DKC·August 18, 2020
Neos Vanadium Excavator Part Number 591/0-6
FDA Recall
Terminated
·Sybron Dental Specialties·Product code EKC·November 14, 2008
Neos Vanadium Excavator Part Number 591/3 SCHE
FDA Recall
Terminated
·Sybron Dental Specialties·Product code EKC·November 14, 2008
Neos Vanadium Excavator Part Number 591/4
FDA Recall
Terminated
·Sybron Dental Specialties·Product code EKC·November 14, 2008
Neos Vanadium Excavator Part Number 591/5 SCHE
FDA Recall
Terminated
·Sybron Dental Specialties·Product code EKC·November 14, 2008
Neos Vanadium Excavator Part Number 591/2
FDA Recall
Terminated
·Sybron Dental Specialties·Product code EKC·November 14, 2008
First Check 1 Panel Drug Cup: (THC); AMT Item Number 990400B
FDA Recall
Terminated
·Ameditech Inc·Product code DKC·August 18, 2020
Neos Vanadium Excavator Part Number 591/0
FDA Recall
Terminated
·Sybron Dental Specialties·Product code EKC·November 14, 2008
Neos Vanadium Excavator Part Number 591/1
FDA Recall
Terminated
·Sybron Dental Specialties·Product code EKC·November 14, 2008
ProScreen" Drugs of Abuse Test (AMT Item/ AMT Description): PSD-6MB/ "ProScreen" Drugs of Abuse Test (MET1000/OPI2000)+AMP+BZO+COC+THC", PSD-6MTDBO-300 /"ProScreen" Drugs of Abuse Test (COC/THC)+BZO+MTD+OPI300+OXY", PSCUP-5M-W/ ProScreen" Drugs of Abuse Cup AMP/COC/MET1000/OPI2000/THC), PSD-10MOB "ProScreen" Drugs of Abuse Test (COC/THC)+(MET1000/OPI2000)+(OXY/ MDMA)+AMP+BZO+BUP+MTD", PSD-5M / "ProScreen" Drugs of Abuse Test AMP/COC/MET1000/OPI2000/THC", PSCUPA-10OM / ProScreen" Drugs of Abuse Cup (COC/THC)+(MET1000/OPI2000)+(OXY/ MDMA) +(PCP/AMP)+BAR+BZO
FDA Recall
Terminated
·Ameditech Inc·Product code DKC·August 18, 2020
LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Cassette in box with foam insert. The cassette is used to check the optics system of the LDX analyzer. Product Usage: The Optics Check Cassette is used to check the optics system of the Alere Cholestech LDX¿ Analyzer. It is run once a day before patient samples are tested and after the analyzer has been moved or serviced.
FDA Enforcement
Class III
·Terminated·Alere San Diego, Inc.·September 21, 2016
GE OEC 9900 Elite ESP fluoroscopic x-ray system. GE Healthcare, Surgery, Salt Lake City, UT. The system is intended to provide an x-ray display of human anatomy.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·August 29, 2008
OEC 9800 Image Intensified fluoroscopic x-ray system (includes OEC 9800, OEC FluoroTrak 9800 Plus, OEC 9800 Plus, and OEC 9800MD Motorized C-arm System), GE Healthcare, Surgery, Salt Lake City, UT.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·April 15, 2008
GE OEC 9800 Fluoroscopic X-Ray System, GE Healthcare, Surgery, Salt Lake City, Utah. The intended use of this device is to perform mobile fluoroscopic examination of human anatomy.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·August 12, 2008
GE OEC 9600 C-arm Fluoroscopy System, GE Healthcare, Surgery, Salt Lake City, Utah.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·July 2, 2008
OEC 9900 Elite Image-intensified fluoroscopic x-ray system (includes OEC 9900 Elite Fluoroscopy System and 9900 EliteMD Motorized C-arm System), GE Healthcare, Surgery, Salt Lake City, UT.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·April 15, 2008