🏥 Medical Devices • 15,809 recalls
Siemens Healthcare Diagnostics
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Siemens Healthcare Diagnostics
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Siemens Healthcare Diagnostics
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Siemens Healthcare Diagnostics
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Sharp Medical Products
Non-conformity (holes/punctures or deep creases) in the sterile barrier.
Tenderneeds Fertility
Device was distributed without a proper marketing authorization.
There is the potential for the Controller power cables (AC Adapter, DC Adapter, and Battery cables), HVAD Alarm Adapter, and HVAD Monitor data cables to cause damage to the HVAD Controller ports when inserting the cables into the Controller ports, due to wear from misalignment of the cables to the port.
Tenderneeds Fertility
Device was distributed without a proper marketing authorization.
ROi CPS, LLC has become aware, through a vendor issued urgent medical device recall notice, that drapes contained within select Regard customer procedure trays may have slits in the product that may lead to a breach in the sterile barrier between fluid in the basin and the slush/warming equipment.
There is the potential for the Controller power cables (AC Adapter, DC Adapter, and Battery cables), HVAD Alarm Adapter, and HVAD Monitor data cables to cause damage to the HVAD Controller ports when inserting the cables into the Controller ports, due to wear from misalignment of the cables to the port.
Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking centrifuge packs during a procedure on the Amicus Separator using therapeutic protocols only. The defect is a blood leak at the boot, elbow, or in the channel on the separation chamber of the centrifuge pack.
Tenderneeds Fertility
Device was distributed without a proper marketing authorization.
Difficulty inserting the biopsy ejector rod into the bone lesion biopsy cannula, preventing the biopsy sample from being collected. Use of a defective device is likely to require immediate repeat biopsy, leading to a prolonged procedure
Device was distributed without a proper marketing authorization.
Terumo Cardiovascular Systems
There is a potential for the stainless steel locking plates on the device's sternal retractor locking mechanism to fracture.
Tenderneeds Fertility
Device was distributed without a proper marketing authorization.
Contact lenses may be mislabeled with the incorrect lens power.
Products show heavy growth of C. albicans after 24 hours of incubation due to misformulation (expected reaction is partial inhibition after 18-48 hours incubation) and reduce the identification of Neisseria contributing to a delay in time to definitive diagnosis or a delay in proper treatment
There is the potential for the Controller power cables (AC Adapter, DC Adapter, and Battery cables), HVAD Alarm Adapter, and HVAD Monitor data cables to cause damage to the HVAD Controller ports when inserting the cables into the Controller ports, due to wear from misalignment of the cables to the port.
Products show heavy growth of C. albicans after 24 hours of incubation due to misformulation (expected reaction is partial inhibition after 18-48 hours incubation) and reduce the identification of Neisseria contributing to a delay in time to definitive diagnosis or a delay in proper treatment