Siemens Medical Solutions USA MAGNETOM Spectra magnetic resonance diagnostic devices Model # recall — FDA Z-2344-2019
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Complete FDA and NHTSA recall records dated in 2019, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
The action is being initiated due to internal testing which identified a possibility for transducers to exceed the acoustic output power (AOP) values defined . The transit voltage values…
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
Battery packs may heat up abnormally and ignite in rare instance.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
QIAsymphony software version 5.0.3 - Software issue incorreclty assigns the 2D bar code eluate ID to the sample within the results file. If 2D bar code eluate IDs are not checked against…
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
Outflow Graft leaking at the pump connection during the implantation process. If the C-Ring is insufficiently seated, it renders the device nonfunctional because the Outflow Graft…
The firm reported that a faulty cutting/punching machine did not meet specifications after being fitted with new blades and did not correctly "notch" BG test strips intended for use in the…
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
The action has been initiated to address reports of burst balloons which have resulted in significant difficulty retrieving the device into the sheath and withdrawing the system from the…
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea,…
Kirkland Signature Three Berry Blend product is recalled due to potential contamination with Hepatitis A virus.
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea,…
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea,…
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.