BD IntelliportRecalls & reported problems across all models

We found 3 models of BD Intelliport by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 30 adverse event reports in the FDA's MAUDE database, received between Feb 3, 2021 and May 26, 2022 — classified as 30 malfunctions.

The most frequently reported specific device problem is “Communication or Transmission Problem” (8 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported BD Intelliport problems

BD Intelliport models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• BD Intelliport 516704

  Infusion safety management software
  28 reports
• BD Intelliport 516700

  Infusion safety management software
  1 report
• BD Intelliport 516701

  Infusion safety management software
  1 report

Recent BD Intelliport adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionMay 26, 2022Wireless Communication Problem; Wireless Communication Problem

  IT WAS REPORTED THAT THE BD INTELLIPORT¿ TABLET KIT FAILED TO TRANSFER THE NEWEST PATIENT DATA BETWEEN CARE AREAS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "USER NOTIFIED THAT THE INTELLIPORT TABLET IS NOT SHOWING THE NEWEST PATIENT THAT WAS SENT BY EPIC. "

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14503579 ↗
• MalfunctionMay 13, 2022Application Program Problem; Application Program Problem

  IT WAS REPORTED THAT THE BD INTELLIPORT¿ TABLET KIT RECORDED A DUPLICATE DOSAGE WHEN THE SYRINGE WAS LEFT ATTACHED FOR 60 SECONDS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "IT WAS REPORTED THAT USER NOTIFIED THAT THE "WEIRD FINDING - LEFT SYRINGE ATTACHED FOR 60 SECONDS - AND IT CAME UP WITH DUPLICATE 60MG ENTRY" ON INTELLIPORT TABLET."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14401371 ↗
• MalfunctionJun 27, 2021Incorrect Measurement; Wireless Communication Problem; Incorrect Measurement; Wireless Communication Problem

  IT WAS REPORTED THAT THE KIT TABLET MEASURED THE AMOUNT OF PROPOFOL INCORRECTLY, AND DID NOT RECORD THE VECURONIUM. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "THE DEVICE MEASURED THE AMOUNT OF PROPOFOL WRONG AND DIDN'T MEASURE THE VECURONIUM AT ALL."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12073077 ↗
• MalfunctionJun 24, 2021Break; Break

  IT WAS REPORTED THAT THE KIT TABLET BASE FAILED, SHOWING A "WAITING FOR THE CASE TO BEGIN" SCREEN DURING THE SURGERY. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CRNA INFORMED ME THAT IPAD WAS NOT WORKING. WHEN I GOT TO THE OR THE SCREEN WAS SHOWING ¿WAITING FOR THE CASE TO BEGIN¿ EVEN THOUGH THE CASE WAS IN THE MIDDLE OF THE SURGERY. THE CASE ENDED FOR CRNA WHEN PROCEDURE STARTED AFTER INDUCTION."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12062945 ↗
• MalfunctionMay 14, 2021Break; Break

  IT WAS REPORTED THAT KIT TABLET SCREEN WENT BLANK. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 516704, BATCH, NO. 20028T02. IT IS REPORTED CUSTOMER WITNESSED SCREEN GO BLANK. VERBIAGE RECEIVED, - "FROM COMPLAINT SECTION IN AN INTELLIPORT PHASE III SURVEY: DATE: (B)(6) 2021, CASE 219, CART-1. "SCREEN WENT BLACK DURING CASE. COULD NOT RESOLVE ON MY OWN. TABLET FULLY CHARGED. NEEDED ASSISTANCE FROM STUDY COORDINATOR".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11829549 ↗
• MalfunctionMay 14, 2021Failure to Read Input Signal; Failure to Read Input Signal

  IT WAS REPORTED THAT KIT TABLET HAD RECORDING ISSUES. THIS OCCURRED ON 2 OCCASIONS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 516704, BATCH NO. 20028T02. IT IS REPORTED CUSTOMER PERFORMANCE ISSUES WITH RECORDING DRUGS AND VOLUMES. VERBIAGE RECEIVED, - "1. DATE: (B)(6) 2021, CASE 218, CART-1, SENSOR 9404. FROM COMMENT SECTION IN AN INTELLIPORT PHASE III SURVEY: "LIDOCAINE DID NOT DETECT FOR UNCLEAR REASON. 08:36 LIDOCAINE 60 MG (3 ML) BUT REGISTERED "VOLUME NOT MEASURED. DOSE GIVEN?" - USER INPUT 3 ML (60 MG) AT 8:38." "2. DATE: (B)(6) 2021, CASE 219, CART-1 SENSOR 9502. FROM COMMENT SECTION IN AN INTELLIPORT PHASE III SURVEY: "PROPOFOL DOSE NOT MEASURED FOR UNCLEAR REASON". 11:51 PROPOFOL 50 MG (5.0 ML) BUT REGISTERED "CONFIRM VOLUME AND DOSE" - USER INPUT 5 ML (50 MG) AT 11:52."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11829443 ↗
• MalfunctionApr 28, 2021Wireless Communication Problem; Wireless Communication Problem

  IT WAS REPORTED THAT KIT TABLET HAD INCORRECT DOSING REPORTED. THIS OCCURRED ON 4 OCCASIONS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 516704 BATCH NO. 20028T02 IT WAS REPORTED THAT "MULTIPLE MEDICATION DOSES DIDN¿T MATCH WHAT WAS GIVEN ON TABLET". VERBIAGE- "MULTIPLE MEDICATION DOSES DIDN¿T MATCH WHAT WAS GIVEN ON TABLET".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11742412 ↗
• MalfunctionApr 23, 2021Battery Problem; Battery Problem

  IT WAS REPORTED THAT KIT TABLET WAS DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 516704, BATCH NO. 20028T01 AND 20028T03. IT WAS REPORTED THAT TABLET HARDWARE AND CABLE WERE DAMAGED DURING USE. VERBIAGE- FROM COMPLAINT SECTION IN AN INTELLIPORT PHASE III SURVEY: DATE: MARCH 25, 2021, CART-2 AND CART-3. "CART 2 USB CABLE WAS DAMAGED IN THE OR. CRNA TEXTED ME THAT TABLET WAS AT 10% BATTERY AND THEN SHUT DOWN. I WENT TO THE OR AND THE USB CABLE WAS DAMAGED RIGHT WHEN IT CONNECTS TO THE TABLET. THE PORT IN THE TABLET IS FINE IT¿S JUST THE USB CABLE. I WAS ABLE TO GRAB ANOTHER CABLE AND TABLET IS CHARGING FINE. NO OTHER ISSUES WITH THE CASE ONCE IT WAS RESENT." "I NOTICED THAT OVER THE WEEKEND TABLET 3 JUST TURNED OFF. I TRIED CHARGING IT AND ALSO SWITCHED OUT THE CABLE FROM DIFFERENT TABLETS, BUT CART 3 TABLET STILL DID NOT TURN ON. I NOTICED THAT SPECIFIC POSITION OF THE CABLE STARTED CHARGING IT, BUT AS SOON AS I LET IT GO IT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11719907 ↗
• MalfunctionApr 16, 2021Failure to Read Input Signal; Failure to Read Input Signal

  IT WAS REPORTED THAT KIT TABLET HAD A SENSOR COMMUNICATION FAILURE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 516704; BATCH NO. 20028T01. IT WAS REPORTED THAT THE SCREEN STATED ¿SENSOR #9702 NOT READY¿ IN RED AND THEN STATED ¿CONTINUE FLUSHING¿ IN YELLOW.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11682604 ↗
• MalfunctionApr 8, 2021Failure to Read Input Signal; Failure to Read Input Signal

  IT WAS REPORTED THAT KIT TABLET HAD PERFORMANCE ISSUES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 516704, BATCH NO. 91DF1F51 AND 4FD8D2B8. IT IS REPORTED CUSTOMER EXPERIENCED PERFORMANCE ISSUES. VERBIAGE RECEIVED, - "FROM COMMENTS SECTION IN A POST MARKET SURVEY: DATE: MARCH 5, 2021, CASE 167, CART-3 3. "NOT AS ACCURATE WITH PICKING UP FENTANYL INJECTED. HAD TO GO BACK A FEW TIMES AND FILL IN."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11638968 ↗
• MalfunctionApr 8, 2021Failure to Read Input Signal; Failure to Read Input Signal

  MATERIAL NO. 516704, BATCH NO. 91DF1F51 AND 4FD8D2B8. IT IS REPORTED CUSTOMER EXPERIENCED PERFORMANCE ISSUES. VERBIAGE RECEIVED, - "FROM COMMENTS SECTION IN A POST MARKET SURVEY: DATE: MARCH 2, 2021, CASE 161, CART-2: 1. "ANCEF CONSISTENTLY STILL INACCURATE. I BELIEVE PROPOFOL TO BE VARIABLE BASED ON USER (VIAL IS OVERFILLED SO IF YOU DRAW UP ALL OF IT, IT TENDS TO BE 210MG IN THE SYRINGE). OTHERWISE NO ISSUES." 2. "OFTEN DOESN¿T REGISTER SUGAMMADEX DOSING."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11638967 ↗
• MalfunctionApr 8, 2021Failure to Transmit Record; Failure to Transmit Record

  IT WAS REPORTED THAT KIT TABLET DID NOT REGISTER THE MEDICATION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 516704, BATCH NO. UNKNOWN. IT IS REPORTED CUSTOMER EXPERIENCED FUNCTIONAL ISSUES WHEN USING TABLET. VERBIAGE RECEIVED, - FROM COMPLAINT SECTION IN A POST MARKET SURVEY: 1. DECADRON FREQUENTLY DOES NOT REGISTER ON TABLET. 2. UNABLE TO CHANGE DOSE ON TABLET.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11638945 ↗
• MalfunctionMar 26, 2021Wireless Communication Problem; Wireless Communication Problem

  IT WAS REPORTED THAT KIT TABLET RECORDED THE INCORRECT DOSAGES. THIS OCCURRED ON 7 OCCASIONS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 516704, BATCH NO. 20028T03 IT IS REPORTED CUSTOMER EXPERIENCED THE RECORDING OF INCORRECT DOSAGES. VERBIAGE RECEIVED, - "CASE #156: TIME 10:20. SENSOR #9450 TABLET: CART-3 10:04 PROPOFOL 160 MG (16.0 ML) BUT REGISTERED 160 MG (16.5 ML) 10:05 VECURONIUM 7 MG (7 ML) BUT REGISTERED 6.5 MG (6.5 ML) 10:16 CEFAZOLIN 1000 MG (10 ML) BUT REGISTERED 900 MG (9 ML) 10:16 CEFAZOLIN 1000 MG (10 ML) BUT REGISTERED 950 MG (9.5 ML) CASE #(B)(4) TIME 13:00. SENSOR #9471 TABLET: CART-3 13:09 PROPOFOL 200 MG (20 ML) BUT REGISTERED 210 MG (21 ML) 13:18 CEFAZOLIN 1000 MG (10.0 ML) BUT REGISTERED 1050 MG (10.5 ML) 14:20 ONDANSTRON HCL 4 MG (2 ML) BUT REGISTERED 2 MG (1 ML)".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11574521 ↗
• MalfunctionMar 17, 2021Failure to Transmit Record; Failure to Transmit Record

  IT WAS REPORTED THAT KIT TABLET RECORDED THE INCORRECT DOSING. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 516704, BATCH NO. 91DF1F51 IT IS REPORTED PRODUCT RECORDED INCORRECT DOSAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11510135 ↗
• MalfunctionMar 16, 2021Failure to Read Input Signal; Failure to Read Input Signal

  IT WAS REPORTED THAT THE KIT TABLET EXPERIENCED INCORRECT DRUG/CONCENTRATION/DOSING REPORTED/RECORDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 516704, BATCH NO. 91DF1F51 DOSE MISMATCH. TIME 08:01. SENSOR #9430 TABLET: CART-2. 08:01 - CEFAZOLIN 1000 MG (TOTAL 2G). CLINICIAN RESEARCH COORDINATOR WHO SUBMITTED THE COMPLAINT STATED THE DOSE REGISTERED AS 1050 MG INSTEAD OF 1000 MG.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11492233 ↗

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