Tuberculosis Antibody Test Card Serum; 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.
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.
Roche Diagnostics Operations
The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502 module of the cobas 8000 modular analyzer series when manually filled cobas c packs are loaded. This issue occurs with tests that use cobas c pack MULTI or empty pre-labeled cobas c packs. The ICVC feature allows the reagent probe to dive into the reagent cassette and confirm the reagent level in the bottles. This ensures
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Energizer Personal Care
Some of the power adapters outer casings may become loose and separate, resulting in a potential for electric shock.
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.
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.
Intuitive Surgical has become aware of the potential for certain lots of the Single-Site 5mm Curved Cannulae to become damaged during use. The second part of this action is to update Single-Site labeling. These labeling changes instruct users how to inspect cannulae prior to use and to appropriately handle cannulae during use.
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.