Morphine Strips (2000); LumiQuick, Santa Clara, CA 95054
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Medical equipment, implants, and diagnostic devices
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
The Male Components in this lot are made of material with lower strength than manufacturing specifications.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Injection port of the Set may leak blood/ IV fluids from the septum of the injection port or the septum may become dislodged
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.