MaxPlus MP1000Recalls & reported problems

Summary

The FDA's MAUDE database contains 43 adverse event reports that list this exact device (DI 10885403232985), received between Sep 17, 2018 and Jun 7, 2026 — classified as 43 malfunctions.

The most frequently reported specific device problem is “Complete Blockage” (21 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, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 43 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 7, 2026Leak/Splash

  IT IS REPORTED, MAXPLUS, LEAK.

  Patient problems: Insufficient Information

  MAUDE report 25422432 ↗
• MalfunctionNov 10, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: DURING THE FLUSHING OF THE IV TUBING ON (B)(6), LIQUID LEAKAGE WAS FOUND AT THE NEEDLELESS CONNECTOR, AND THE PRODUCT WAS REPLACED.

  Patient problems: Insufficient Information

  MAUDE report 23513635 ↗
• MalfunctionNov 5, 2025Leak/Splash; Leak/Splash

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23480768 ↗
• MalfunctionNov 5, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT BD MAXPLUS NEEDLESS CONNECTOR WAS LEAKING. THE FOLLOWING INFORMATION WAS RECEIVED BY THE INITIAL REPORTER WITH THE FOLLOWING VERBATIM: IT WAS REPORTED BY A CUSTOMER THAT THE CHEMO LEAKING FROM WHERE CONNECTOR MEETS PICC LINE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23480131 ↗
• MalfunctionOct 27, 2025Leak/Splash; Leak/Splash

  EVENT DETAILS: CHEMO LEAKING FROM WHERE CONNECTOR MEETS PICC LINE. PATIENT WALKING THROUGH THE HALLWAY AND CHEMO LEAKED SLOWLY OUT OF THE LINE. ITEM - 515052.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23392308 ↗
• MalfunctionSep 8, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: I DISCOVERED A LEAK IN THE CONNECTOR DURING USE. ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER: PLEASE CONFIRM WHETHER THE LEAKAGE WAS DETECTED DURING THE PRIMING STAGE OR DURING INFUSION. IF DURING INFUSION, PLEASE SPECIFY THE EXACT INFUSION TIME. = LEAKAGE WAS OBSERVED DURING BOTH PRIMING AND INFUSION STAGES. THE LEAKAGE OCCURRED INTERMITTENTLY OVER THE PAST MONTH; THE EXACT INFUSION TIME IS UNKNOWN. PLEASE CONFIRM THE SUBSTANCES INFUSED. = GLUCOSE SOLUTION, AMINO ACIDS, CISPLATIN, ETC. PLEASE CONFIRM THE BRAND AND MODEL OF THE CONNECTING PRODUCT. = CANNULA-FREE CONNECTOR MP1000. PLEASE CONFIRM THE QUANTITY OF AFFECTED PRODUCTS. = 50 VIALS. PLEASE CONFIRM WHETHER THE PRE-ASSEMBLY COMPONENTS WERE STERILISED PRIOR TO CONNECTION. IF SO, PLEASE SPECIFY THE STERILISING AGENT USED. = STERILISED. POVIDONE-IODINE. PLEASE CONFIRM WHETHER THE PRODUCT EXHIBITS ANY DAMAGED. = NONE. PLEASE PROVIDE DETAILS OF PRE-USE STORAGE CONDITIONS: WHERE WAS THE PRODUCT STORED? WAS THE STORAGE AREA TEMPERATURE-CONTROLLED? = STO

  Patient problems: Insufficient Information

  MAUDE report 22998509 ↗
• MalfunctionAug 15, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: DURING THE INTRAVENOUS INFUSION OF THE PATIENT'S RIGHT KNEE MENISCUS INJURY AFTER SURGERY, IT WAS FOUND THAT THE LIQUID WAS NOT DRIPPING. AFTER REPEATED CHECKS, THE LIQUID DRIPPED SMOOTHLY AFTER REPLACING THE CONNECTOR.

  Patient problems: Insufficient Information

  MAUDE report 22821556 ↗
• MalfunctionAug 5, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: ON (B)(6), 2025, DURING POSTOPERATIVE INFUSION, A NURSE DISCOVERED A BLOCKAGE IN THE NEEDLELESS CONNECTOR WHILE USING IT. THE NURSE IMMEDIATELY REPLACED THE CONNECTOR AND CONTINUED THE PROCEDURE. NO HARM WAS CAUSED TO THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22716989 ↗
• MalfunctionJul 31, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: ON (B)(6) 2025, AT 8:30 AM, THE PATIENT WAS ADMITTED TO THE HOSPITAL. HER PICC LINE WAS DUE FOR MAINTENANCE, REQUIRING A NEEDLELESS CONNECTOR REPLACEMENT. AFTER PREPARING THE NECESSARY SUPPLIES AND BEGINNING THE PROCEDURE, THE CONNECTOR WAS FOUND TO BE CLOGGED, PREVENTING SALINE INJECTION. A NEW CONNECTOR WAS IMMEDIATELY REPLACED TO AVOID DELAYING THE MAINTENANCE. THE PATIENT UNDERWENT MAINTENANCE WITHOUT ANY PROBLEMS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22672888 ↗
• MalfunctionJul 15, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: THE PATIENT SUFFERED FROM CEREBRAL INFARCTION AND RECEIVED INTRAVENOUS INFUSION USING A NEEDLE-FREE CONNECTOR AT 16:00 ON (B)(6) 2024. THE CONNECTOR OF THE PRODUCT WAS BLOCKED AND THE PATIENT WAS NOT HURT, SO IT WAS REPLACED IMMEDIATELY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22512108 ↗
• MalfunctionJul 15, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: PATIENT RECEIVED A BLOOD TRANSFUSION FROM A BLOOD TRANSFUSION DEVICE AT 11:29 ON (B)(6) 2024 DUE TO ACUTE MYELOID LEUKEMIA. WHEN THE NORMAL SALINE WAS CONNECTED, THE LIQUID FLOWED SMOOTHLY. WHEN THE PLATELETS WERE REPLACED, IT WAS FOUND THAT THE PLATELETS DID NOT DRIP. AFTER INSPECTION, IT WAS FOUND THAT THE NEEDLELESS CONNECTOR WAS BLOCKED. NO HARM WAS CAUSED TO THE PATIENT, SO IT WAS REPLACED IMMEDIATELY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22509226 ↗
• MalfunctionJul 14, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: PATIENT USED A BLOOD TRANSFUSION DEVICE TO RECEIVE PLASMA AT 17:11 ON (B)(6) 2025. WHEN CONNECTED TO NORMAL SALINE, THE LIQUID FLOWED SMOOTHLY. WHEN REPLACED WITH PLASMA, IT WAS FOUND THAT THE PLASMA DID NOT DRIP. AFTER INSPECTION, IT WAS FOUND THAT THE NEEDLELESS CONNECTOR WAS BLOCKED. NO HARM WAS CAUSED TO THE PATIENT, AND IT WAS REPLACED IMMEDIATELY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22503765 ↗
• MalfunctionJul 14, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: THE PATIENT WAS ADMITTED TO THE HOSPITAL DUE TO MALIGNANT TUMOR OF GALLBLADDER. WHEN HE USED THE INFUSION SET FOR INFUSION ON (B)(6) 2025, THE LIQUID STATIC POINT WAS UNOBSTRUCTED. THEN WHEN HE CHANGED TO A BLOOD TRANSFUSION SET, THE LIQUID DID NOT DRIP. AFTER CHANGING THE BLOOD TRANSFUSION SET AGAIN, THE LIQUID STILL DID NOT DRIP. AFTER REPLACING THE NEEDLELESS CONNECTOR, THE LIQUID STATIC POINT WAS UNOBSTRUCTED. ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER: PLEASE CONFIRM WHEN WAS THE ISSUE IDENTIFIED? DURING PRIMING OR INFUSION? AFTER CONNECTION IS COMPLETED. PLEASE CONFIRM WHAT MEDICATION WAS BEING ADMINISTERED DURING THE EVENT? UNABLE TO CONFIRM. PLEASE CONFIRM IF THE MEDICATION WAS STORED IN THE REFRIGERATOR? IF YES, WAS IT ALLOWED TO REACH ROOM TEMPERATURE BEFORE USE? ROOM TEMPERATURE 22-24 DEGREES. PLEASE CONFIRM THE MAKE AND MODEL OF THE CONNECTING PRODUCTS? WEIGAO. PLEASE CONFIRM IF THERE ARE ANY VISIBLE DEFECTS TO THE DEVICE I.E., CRACKS, FLASHES, KINKS? NONE. PLEASE CONFIRM IF THE CONNECTIN

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22502689 ↗
• MalfunctionJul 14, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: PATIENT RECEIVED A BLOOD TRANSFUSION FROM A BLOOD TRANSFUSION DEVICE AT 17:40 ON (B)(6) 2025 DUE TO ACUTE MYELOID LEUKEMIA. WHEN CONNECTED TO NORMAL SALINE, THE LIQUID FLOWED SMOOTHLY. WHEN REPLACED WITH SUSPENDED RED BLOOD CELLS, IT WAS FOUND THAT THE DRIP SPEED WAS SLOW. AFTER INSPECTION, IT WAS FOUND THAT THE NEEDLELESS CONNECTOR WAS BLOCKED. NO HARM WAS CAUSED TO THE PATIENT, SO IT WAS REPLACED IMMEDIATELY. ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER: PLEASE CONFIRM THE BLOCKAGE WAS COMPLETELY OR PARTIAL? COMPLETE PLEASE CONFIRM THE MAKE AND MODEL OF THE CONNECTING PRODUCTS? WEIGAO PLEASE CONFIRM IF THERE ARE ANY VISIBLE DEFECTS TO THE DEVICE I.E., CRACKS, FLASHES, KINKS? NO.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22502327 ↗
• MalfunctionJul 14, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: DUE TO FATIGUE, THE PATIENT WAS GIVEN INFUSION TREATMENT USING A NEEDLE-FREE CONNECTOR CONNECTED TO AN INDWELLING NEEDLE INFUSION SET AT 11:00 ON (B)(6) 2025. IT WAS FOUND THAT THE LIQUID DID NOT FLOW SMOOTHLY AFTER THE NEEDLE-FREE CONNECTOR WAS CONNECTED. AFTER THE NEEDLE-FREE CONNECTOR WAS REPLACED, THE LIQUID FLOWED SMOOTHLY. ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER: PLEASE CONFIRM WHEN WAS THE ISSUE IDENTIFIED? DURING PRIMING OR INFUSION? WHEN PRIMED. PLEASE CONFIRM WHAT MEDICATION WAS BEING ADMINISTERED DURING THE EVENT? UNABLE TO RECALL. PLEASE CONFIRM IF THE MEDICATION WAS STORED IN THE REFRIGERATOR? IF YES, WAS IT ALLOWED TO REACH ROOM TEMPERATURE BEFORE USE? RECOVERED AT ROOM TEMPERATURE. PLEASE CONFIRM THE MAKE AND MODEL OF THE CONNECTING PRODUCTS? WEIGAO. PLEASE CONFIRM IF THERE ARE ANY VISIBLE DEFECTS TO THE DEVICE I.E., CRACKS, FLASHES, KINKS? NO PLEASE CONFIRM IF THE CONNECTING PRODUCT HAS A LUER SLIP OR LUER LOCK CONNECTION? LUER CONNECTOR. PLEASE CONFIRM WHETHER THE FLOW WAS COMPLET

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22501099 ↗
• MalfunctionJul 14, 2025Defective Component; Defective Component

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR IS DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: THE PATIENT WAS GIVEN INTRAVENOUS INFUSION AT 9:30 ON (B)(6) 2025, AND IT WAS FOUND THAT THE LIQUID WAS NOT DRIPPING DURING THE INFUSION. AFTER REPEATED INSPECTION, THE INNER CORE OF THE NEEDLELESS CONNECTOR DID NOT REBOUND. AFTER REPLACING THE CONNECTOR, THE LIQUID DRIPPED SMOOTHLY. ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER: HAS THERE BEEN ANY LEAKAGE CAUSED DUE TO THE DIFFICULTY IN PISTON REBOUND? NONE PLEASE CONFIRM THE MAKE AND MODEL OF THE CONNECTING PRODUCT(AS)? UNABLE TO OBTAIN PLEASE CONFIRM IF THERE IS ANY VISIBLE DAMAGE ON THE SET ¿ SUCH AS CRACKS, FLASHES OR DEFORMATION OF THE PISTON? THE CUSTOMER CANNOT REMEMBER PLEASE CONFIRM WHAT SUBSTANCE WAS BEING INFUSED DURING THE TIME OF THE EVENT? THE CUSTOMER CANNOT REMEMBER PLEASE CONFIRM HOW LONG INTO THE INFUSION BEFORE TO THE ISSUE NOTICED? UNABLE TO OBTAIN PLEASE CONFIRM IF THE COMPONENT WAS ACCESSED WITH A NEEDLE THEN REUSED? NO PLEASE CONFIRM THE CONDITION OF THE STORAGE ¿ TEMPERATURE, HUMIDITY ETC? ROOM TEMPERATURE 22 DEGREES PLEASE CONFIR

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22500863 ↗
• MalfunctionJun 10, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS NEEDLELESS CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: THE PATIENT WAS GIVEN INTRAVENOUS INFUSION AT 09:00 ON (B)(6) 2024, AND IT WAS FOUND THAT THE LIQUID WAS NOT DRIPPING. AFTER REPEATED CHECKS, THE LIQUID DRIPPED SMOOTHLY AFTER REPLACING THE CONNECTOR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22178880 ↗
• MalfunctionMay 16, 2025Defective Component; Defective Component

  IT WAS REPORTED THAT THE BD MAXPLUS POSITIVE PRESSURE CONNECTOR WAS DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: DURING THE USE OF THIS PRODUCT, THE PISTON JOINT FAILED TO REBOUND.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22040821 ↗
• MalfunctionApr 10, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS NEEDLELESS CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM CHINESE TO ENGLISH: DURING THE INTRAVENOUS INFUSION AT 09:00 ON (B)(6) 2024, IT WAS FOUND THAT THE LIQUID WAS NOT DRIPPING. AFTER REPEATED INSPECTIONS AND REPLACEMENT OF THE CONNECTOR, THE LIQUID DRIPPED SMOOTHLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21819927 ↗
• MalfunctionMar 20, 2025Complete Blockage; Complete Blockage

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21657635 ↗
• MalfunctionJan 16, 2025Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT THE BD MAXPLUS NEEDLELESS CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE PATIENT WAS SEEN AT OUR HOSPITAL FOR 11 HOURS FOR CHEST COMPRESSION AND WAS GIVEN FLUIDS ON (B)(6) 2024, AS PRESCRIBED, AND AFTER USING AN INFUSION SET CONNECTED TO A NEEDLELESS CONNECTOR, THE FLUIDS DID NOT PASS THROUGH, AND A REPLACEMENT NEEDLELESS CONNECTOR WAS GIVEN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21170352 ↗
• MalfunctionDec 29, 2024Complete Blockage; Complete Blockage

  IT WAS REPORTED THAT BD MAXPLUS NEEDLELESS CONNECTOR WAS OCCLUDED. THE FOLLOWING INFORMATION WAS RECEIVED BY THE INITIAL REPORTER WITH THE FOLLOWING VERBATIM ON (B)(6) 2024 AT 0900 HOURS DURING THE COURSE OF GIVING IV FLUIDS IT WAS NOTED THAT THE FLUIDS WERE NOT DRIPPING, REPEATED CHECKS WERE MADE, AND AFTER CHANGING THE CONNECTOR THE FLUIDS WERE STATIC AND SMOOTH.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21032746 ↗
• MalfunctionDec 13, 2024Partial Blockage; Complete Blockage; Partial Blockage; Complete Blockage

  IT WAS REPORTED THAT BD MAXPLUS NEEDLELESS CONNECTOR WAS OCCLUDED THE FOLLOWING INFORMATION WAS RECEIVED BY THE INITIAL REPORTER WITH THE FOLLOWING VERBATIM PATIENT DIAGNOSED WITH MYELODYSPLASTIC SYNDROMES, ON (B)(6) 2024 USING AN INDWELLING NEEDLE CONNECTED TO A NEEDLELESS CONNECTOR FOR INFUSION THERAPY, CONNECTING THE FLUID WAS NOT SMOOTH, MULTIPLE ATTEMPTS WERE MADE TO FIND THAT THE NEEDLELESS CONNECTOR WAS CLOGGED AND COULD NOT BE USED PROPERLY, REPLACED WITH A NEW NEEDLELESS CONNECTOR, THE FLUID WAS USUALLY, AND THE INFUSION THERAPY WAS CONTINUED WITHOUT CAUSING HARM TO THE PATIENT

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20921852 ↗
• MalfunctionDec 7, 2024Leak/Splash; Leak/Splash

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20873770 ↗
• MalfunctionOct 22, 2024Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT BD MAXPLUS NEEDLELESS CONNECTOR WAS LEAKING THE FOLLOWING INFORMATION WAS RECEIVED BY THE INITIAL REPORTER WITH THE FOLLOWING VERBATIM THE PATIENT WAS ADMITTED TO THE HOSPITAL WITH OSTEOARTHRITIS OF THE KNEE AND WAS FOUND TO BE LEAKING FLUID DURING THE COURSE OF AN IV INFUSION GIVEN AT 18:00 ON (B)(6) 2024, AND WAS VIEWED TO BE LEAKING AT THE NEEDLELESS CONNECTOR, AND WAS GIVEN A NEW NEEDLELESS CONNECTOR WITH NO LEAKAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20511452 ↗