Smiths Medical BCI Autocorr Plus

Technical Specs

Height

3.5 in

Length

5.5 in

Pulse Rate Range

30-254 BPM

Weight

5 lbs

SpO2 Range

0-100%

Width

10 in

Typical Location

Where this class of equipment is typically deployed - general reference, not this unit's own placement record.

• ICU / CCU
• Emergency Department
• OR / PACU
• General med-surg floors
• Step-down units
• Telemetry units

Documents & Manuals

• User ManualUser Manual · External
• Autocorr Plus BrochureBrochure · External

Safety & Recalls

Synced live from the FDA openFDA API.

• RECALL

  Airway adapter does not meet specification and may break off when attaching a valve or tube. Device failure may result in inaccurate readings, a break in airway circuit, and loss of ventilation. A break in the airway circuit could result in inability to ventilate, hypoxia, cardiopulmonary collapse, or death.

• RECALL

  There is a potential for inadvertent tidal volume knob movement from the original setting when set at high (1000-1500 mL) and low (70-150 mL) settings.

• RECALL

  Smiths Medical became aware of an issue related to a potential for the patient outlet connector to loosen/detach from the paraPAC Plus P300 and P310 ventilators impacting the active ventilation function.

• RECALL

  Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defect.

• RECALL

  When a paraPAC plus ventilator is switched to the operating mode of VENTILATE, the ventilator may intermittently provide continuous positive gas flow instead of the intended cycling like a human breath. This non-cycling and continuous positive gas flow when in the cycling mode, is a malfunction, not allowing the ventilator to properly function as designed.

• RECALL

  Two devices were labeled with the same serial number

• RECALL

  Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.

• RECALL

  Certain lots of the Model 306701 ProtectIV Plus Safety IV Catheter may exhibit damage on the safety mechanism guard.

• RECALL

  In rare instances, the BCI Remote Alarm Cables (BCI Cable) are not transferring alarms when used with some remote nurse alarm systems.

• RECALL

  Difficulty disconnecting accessories from the Bivona Uncuffed Neonatal, Pediatric and Flextend Tracheostomy Tubes TR3 connector, which may result in a delay in initiating therapy or patient discomfort. If excessive force is used to detach the accessory, this may result in decannulation of the tube which could result in serious injury or death; especially if no replacement tracheostomy tube is imm

• RECALL

  Due to a component that may be installed backwards, the device may turn off or may immediately reset.

• RECALL

  Phantom pacer spikes caused by a damaged resistor.

• RECALL

  An error occurred at the board manufacturing site which may affect the following parameters: - An electrical noise observed on the SpO2 pleth waveform generating and displaying erratic heart rates. % SpO2 reading displays dashes. - The ECG waveform may appear noisy, ECG readings appear accurate. -Respiration waveform may appear noisy and the respiration readings will be displayed as dashes.

• RECALL

  Smiths Medical became aware that product returned to them under recall # Z-0800-06/ Z-0807-06 was inadvertently distributed to consignees after the recall was initiated 03/29/2006. The product was originally recalled because Locator Wand covers, which are supplied on the outside of PORT-A-CATH and P.A.S. PORT sterile trays, may have an insufficient seal and product sterility could be compromised.

• RECALL

  One lot of Locator-Wand Cover sterile pouches may have an insufficient seal and product sterility could be compromised. The Locator-Wand Cover is supplied with the PORT-A-CATH II AND P.A.S. PORT systems. The packaged Wand-Cover is placed on the outside of the PORT-A-CATH II AND P.A.S. PORT tray.