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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

Higher than published scatter around the probe head when testing some samples. At the point the customer would interact directly with the instrument (Trigger position), most readings were lower. However, measurements around the probe head were higher particularly on samples know to be highly scattering (plastics, soils) with minimal increases on high density samples (steel, aluminum).

Jun 9, 2015 Other Medical Devices Nationwide View Details →

The affected S2 fluid packs may generate a transponder error when the fluid pack is loaded on to the cobas b 221 system. The error prevents the fluid from being recognized by the system and the instrument cannot start measurements until the affected S2 Fluid Pack is replaced.

Jun 24, 2015 Diagnostic Equipment View Details →

The adhesive between the sphere assembly and the biopsy needle shaft may be compromised, causing the sphere assembly to move on the needle shaft. This may result in inaccurate navigation and improper placement of the needles biopsy window in the brain.

Jul 17, 2015 Surgical Instruments Nationwide View Details →

Reports of catheter tip splits and or separation. Loss of device function, medical intervention to retrieve separated segment, or complications resulting from separated tip occluding blood flow to end organs may result.

Jul 2, 2015 Surgical Instruments Nationwide View Details →

The inside of the folded Instructions For Use (IFU) pamphlet was missing the usage instructions and warnings.

Jun 24, 2015 Surgical Instruments Nationwide View Details →

Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking bone screw collars not 'locking'.

Jul 20, 2015 Implants & Prosthetics View Details →

The possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate the components inside the table. If this occurs, table movements may no longer be possible. No injuries reported.

Jun 29, 2015 Diagnostic Equipment Nationwide View Details →

A system freeze-up of the Merge Hemo system, that included the PHASEIN End Tidal CO2 unit, resulted in the user needing to move the patient to another cath lab.

Jan 21, 2015 Diagnostic Equipment Nationwide View Details →

The adhesive between the sphere assembly and the biopsy needle shaft may be compromised, causing the sphere assembly to move on the needle shaft. This may result in inaccurate navigation and improper placement of the needles biopsy window in the brain.

Jul 17, 2015 Surgical Instruments Nationwide View Details →

A gradient cable in the ACGD cabinet may be missing a spacer that prevents connecting the gradient cable terminals in the wrong polarity on X gradient amplifier. This could cause images to be flipped left-right with incorrect orientation annotation.

Jul 10, 2015 Diagnostic Equipment Nationwide View Details →

When using the CIVCO biopsy attachments in combination with the ACUSON S Family on-screen guidelines, the biopsy needle may traverse outside the on-screen guidelines.

Jun 29, 2015 Diagnostic Equipment Nationwide View Details →

The inside of the folded Instructions For Use (IFU) pamphlet was missing the usage instructions and warnings.

Jun 24, 2015 Surgical Instruments Nationwide View Details →