Webcol 5110Recalls & reported problems

Summary

The FDA's MAUDE database contains 16 adverse event reports that list this exact device (DI 10192253046205), received between Mar 11, 2026 and Jun 1, 2026 — classified as 16 injuries.

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 16 most recent of 16 reports, in the reporter's own words as published by the FDA.

• InjuryJun 1, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED VIA MEDWATCH THAT THE REPORTER'S DAUGHTER STARTED DEVELOPING A RASH ON HER ARM ON (REDACTED BY FDA) 2026. THIS GOT INCREASINGLY WORSE AND THEY SOUGHT MEDICAL HELP. THEY WERE LATER INFORMED VIA AMAZON ABOUT THE WEBCOL ALCOHOL WIPES AND THIS IS HOW THEY CONNECTED THE DOTS. ADDITIONAL INFORMATION RECEIVED ON 15MAY2026 STATED THAT THEY ARE NOT SURE WHAT THE LOT NUMBER IS. THE PATIENT WAS SEEN BY A DERMATOLOGIST AND THEY DID PRESCRIBE MOMETASONE CREAM. HOWEVER, THEY DIDN¿T USE THE CREAM AS THE RASH STARTED CLEARING WITH HOME REMEDIES USED.

  Patient problems: Rash

  MAUDE report 25355442 ↗
• InjuryMay 22, 2026Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED THAT SHE PURCHASED OUR PRODUCT THAT IS RECALLED. SHE HAS STOPPED USING THEM. SHE STATED THAT SHE HAD A REACTION A COUPLE OF TIMES WHEN SHE SELF-INJECTED DIABETES MEDICATION THAT WAS NOT NORMAL. SHE GOT INFLAMED AND ITCHY WITH RED SPLOTCHES. SHE HAS SINCE STOPPED USING THE PRODUCT. PER THE INITIAL REPORTER ON 05MAY2026, SHE THREW THE PRODUCT OUT ONCE SHE SAW THE NOTICE SO SHE DOES NOT HAVE THE LOT NUMBER OR SAMPLES. SHE SAID SHE DID NOT REQUIRE ANY MEDICAL INTERVENTION BEYOND NEOSPORIN AND CORTISONE, WHICH SHE HAD ON HAND.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 25254983 ↗
• InjuryMay 14, 2026Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED THAT HER HUSBAND WAS DIAGNOSED WITH STAGE 4 BILE DUCT CANCER. IN THE FALL OF LAST YEAR, HE STARTED HAVING REALLY SERIOUS INFECTIONS THAT BROUGHT HIM REPEATEDLY TO (B)(6). THE MOST SERIOUS WAS SEPSIS AND THEY THOUGHT THEY LOST HIM ON THAT VISIT. THEY FOUND OUT ABOUT THE RECALL OF THE ALCOHOL WIPES AND WAS ASTOUNDED. AT ONE POINT SHE WAS GIVING HIM ANTIBIOTICS THROUGH HIS PICC LINE 5X A DAY PLUS HIS TPN. FAITHFULLY SHE WOULD USE OUR WIPES. WHEN THEY STOPPED USING THE WIPES, THE INFECTIONS ALSO STOPPED. THE CUSTOMER STATED THAT THEIR TIME WITH HER HUSBAND IS SO PRECIOUS. HE HAD BEEN ABLE TO WORK REMOTELY UNTIL THE CONSTANT HOSPITALIZATIONS MADE IT IMPOSSIBLE! SHE WAS UNABLE TO WORK, HIS TWIN SISTER AS WELL AND HER DAUGHTER HAS HAD TO PUT HER LIFE ON HOLD REPEATEDLY TO WATCH THEIR HOUSEHOLD WHILE THEY WERE HOSPITALIZED. WHAT WAS TAKEN FROM THEM CANNOT BE MEASURED. SHE STATED THAT OUR COMPANY SHOULD BE ASHAMED FOR THE MAIN AUDIENCE BEING AFFECTED BY THIS BEING THOSE WITH COMPROMISED IMMUNE SYSTEMS. THERE WAS PAPERWORK SENT WITH THEIR SUPPLIES BUT IRONICALLY, THEY WERE AT AN EMERGENCY TRIP TO THE HOSPITAL AND MISSED IT. AND HOW DID IT TAKE SO LONG WHEN THE INITIAL D

  Patient problems: Sepsis; Unspecified Infection

  MAUDE report 25179099 ↗
• InjuryApr 30, 2026Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED THAT HER HUSBAND WAS DIAGNOSED WITH STAGE 4 BILE DUCT CANCER. IN THE FALL OF LAST YEAR HE STARTED HAVING REALLY SERIOUS INFECTIONS THAT BROUGHT HIM REPEATEDLY TO (B)(6) IN (B)(6). THE MOST SERIOUS WAS SEPSIS AND THEY THOUGHT THEY LOST HIM ON THAT VISIT. THEY FOUND OUT ABOUT THE RECALL OF THE ALCOHOL WIPES AND WAS ASTOUNDED. AT ONE POINT SHE WAS GIVING HIM ANTIBIOTICS THROUGH HIS PICC LINE 5X A DAY PLUS HIS TPN. FAITHFULLY SHE WOULD USE OUR WIPES. WHEN THEY STOPPED USING THE WIPES, THE INFECTIONS ALSO STOPPED. THE CUSTOMER STATED THAT THEIR TIME WITH HER HUSBAND IS SO PRECIOUS. HE HAD BEEN ABLE TO WORK REMOTELY UNTIL THE CONSTANT HOSPITALIZATIONS MADE IT IMPOSSIBLE! SHE WAS UNABLE TO WORK, HIS TWIN SISTER AS WELL AND HER DAUGHTER HAS HAD TO PUT HER LIFE ON HOLD REPEATEDLY TO WATCH THEIR HOUSEHOLD WHILE THEY WERE HOSPITALIZED. WHAT WAS TAKEN FROM THEM CANNOT BE MEASURED. SHE STATED THAT OUR COMPANY SHOULD BE ASHAMED FOR THE MAIN AUDIENCE BEING AFFECTED BY THIS BEING THOSE WITH COMPROMISED IMMUNE SYSTEMS. THERE WAS PAPERWORK SENT WITH THEIR SUPPLIES BUT IRONICALLY THEY WERE AT AN EMERGENCY TRIP TO THE HOSPITAL AND MISSED IT. AND HOW DID IT TAKE SO LONG WHEN THE I

  Patient problems: Sepsis; Unspecified Infection

  MAUDE report 25045795 ↗
• InjuryApr 30, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED VIA MEDWATCH THAT THE REPORTER'S HUSBAND HAS RHEUMATOID ARTHRITIS (SINCE 2009) AND TAKES BIWEEKLY ACTEMRA INJECTIONS WHICH HE RECEIVES FROM (B)(6) HOSPITAL SPECIALTY PHARMACY IN (REDACTED BY FDA). HIS MEDICATIONS ARRIVE WITH WEBCOL LARGE ALCOHOL PREP PADS TO CLEAN THE SKIN PRIOR TO INJECTION. HIS LAST USE OF THE WEBCOL ALCOHOL PAD WAS (REDACTED BY FDA) 2026 WITH HIS ACTEMRA INJECTION. HE EXPERIENCED SUDDEN EXCRUCIATING BACK PAIN ON (REDACTED BY FDA) 2026. HE WAS URGENTLY ADMITTED TO THE (REDACTED BY FDA) CLINIC FOUNDATION AND DIAGNOSED WITH BACTEREMIA, OSTEOMYELITIS, DISCITIS, SPINAL AND PSOAS MUSCLE ABSCESS. ON (REDACTED BY FDA) 2026, THE REPORTER RECEIVED AN EMAIL FROM (B)(6) HOSPITAL SPECIALTY PHARMACY WHILE SITTING BEDSIDE WITH HER HUSBAND IN CRITICAL CONDITION THAT THE FDA RECALLED THE WEBCOL ALCOHOL PREP PADS AND THEY SHOULD "DISPOSE OF THEM IMMEDIATELY AND DO NOT USE THEM." HER HUSBAND HAS HAD MULTIPLE BLOOD TESTS SHOWING BACTEREMIA AND SEPSIS LACTATE. REASON FOR USE: TO CLEAN SKIN AREA PRIOR TO INJECTIONS OF ACTEMRA. THE FDA RECALL ANNOUNCEMENT WAS ATTACHED TO THEIR EMAIL. THE REPORTER'S HUSBAND'S SYMPTOMS STARTED ON (REDACTED BY FDA) 2026 AND HE WAS ADMITTE

  Patient problems: Abscess; Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Back pain; Bacteremia; Osteomyelitis; Sepsis

  MAUDE report 25045584 ↗
• InjuryApr 28, 2026Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED THAT THE PATIENT RECEIVED A VYEPTI INFUSION AT HOME BY OPTION CARE HEALTH. THE WEBCOL ALCOHOL PREP PADS USED TO PREPARE FOR THE INFUSION NEEDLE WAS ONE OF THE RECALLED BOXES. THE PATIENT HAD A RED RASH GO UP HER ARM A COUPLE OF DAYS AFTER THE INFUSION WHICH WAS ON (B)(6) 2026. THE RASH WAS APPROXIMATELY AN INCH WIDE AND ALMOST ENCIRCLED HER ARM JUST ABOVE THE INFUSION SITE. HER PCP PUT HER ON TWO ANTIBIOTICS, AND IT TOOK TWO WEEKS TO GET IT ALMOST CLEARED UP. ON (B)(6) 2026, THE CUSTOMER STATED THAT THE VYEPTI WAS ADMINISTERED TO ADDRESS MIGRAINE HEADACHES. THE RASH APPEARED FOLLOWING THE ADMINISTRATION OF THE VYEPTI. ONE ANTIBIOTIC GIVEN TO ADDRESS THE RASH WAS DOXYCYCLINE BUT SHE IS NOT CERTAIN ABOUT THE OTHER.

  Patient problems: Rash

  MAUDE report 25023950 ↗
• InjuryApr 28, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED ANONYMOUSLY VIA MEDWATCH THAT (REDACTED BY FDA) SENT THE REPORTER SOME OF THE RECALLED WEBCOL ALCOHOL WIPES TO MAINTAIN STERILITY IN THEIR CENTRAL LINE. DUE TO THIS RECALL, THE REPORTER DEVELOPED A BLOODSTREAM INFECTION AND DEALT WITH SYMPTOMS LEAVING THEM WITHOUT NUTRITION OR HYDRATION FOR 3 WEEKS, AND WAS ADMITTED TO THE HOSPITAL FOR 10 DAYS. NO ADDITIONAL INFORMATION CAN BE OBTAINED FROM THE REPORTER BECAUSE THE EVENT WAS REPORTED ANONYMOUSLY TO FDA.

  Patient problems: Unspecified Infection

  MAUDE report 25023811 ↗
• InjuryApr 28, 2026Adverse Event Without Identified Device or Use Problem

  ON (B)(6) 2026, THE CUSTOMER LEFT A MESSAGE WITH THE FIELD CORRECTION ACTION TEAM STATING THAT SHE RECEIVED A LETTER ABOUT HER ALCOHOL PREPS BEING POSSIBLY ON THE RECALL AND THEN CONFIRMED THAT THEY ARE BECAUSE THE LOT NUMBER MATCHES. SHE STATED SHE GOT AN INFECTION A COUPLE OF DAYS AFTER USING THEM WHICH THEY HAD TO CUT HER OPEN TO DRAIN IT. DURING A CALL BACK ON (B)(6) 2026, THE CUSTOMER STATED THAT SHE DOES IMMUNOGLOBULIN (IGG) THERAPY. SHE CLEANED THE INJECTION SITE WITH THE AFFECTED PREP PADS PRIOR TO STICKING HERSELF WITH THE NEEDLE AND NOT EVEN A DAY OR SO LATER, IT BECAME PUFFY. SHE STATED THE INJECTION SITES TYPICALLY GET PUFFY, BUT THIS SITE STAYED PUFFY WHILE THE OTHER SITES GO DOWN. SHE ALSO STATED THAT THE SITE GOT STREAKS OF RED, WAS HOT AND HARD LIKE A KNOT. SHE CALLED HER DOCTOR AND DID A TELEHEALTH VISIT WITH URGENT CARE. THEY GAVE HER ANTIBIOTICS. THE SITE CONTINUED TO GET WORSE. SHE CALLED HER IMMUNOLOGIST WHO STATED SHE MAY NEED TO GET THE SITE CUT OPENED FOR DRAINAGE. SHE WENT TO AN URGENT CARE FACILITY, AND THEY CUT OPEN THE SITE WITH A SCALPEL, AND LEFT IT OPEN FOR DRAINAGE. SHE RECEIVED A 2ND DOSE OF ANTIBIOTICS. SHE WAS REQUIRED TO PRESS ON THE WOUND TO SQU

  Patient problems: Unspecified Infection

  MAUDE report 25021766 ↗
• InjuryApr 3, 2026Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED THAT UNFORTUNATELY, THEY HAVE BEEN USING THIS PRODUCT ON AN INDIVIDUAL WHO HAS CANCER, IS RECEIVING CHEMO AND IMMUNOCOMPROMISED AND WAS RECENTLY HOSPITALIZED FOR INFECTION. ADDITIONAL INFORMATION PROVIDED BY THE CUSTOMER AND STATED THAT THE PATIENT BEGAN USING WEBCOL WIPES ON MARCH 7, 2026. ON MARCH 16, 2026, THE PATIENT DEVELOPED SYMPTOMS OF NEUTROPENIC FEVER AND WAS HOSPITALIZED DUE TO AN ENTEROCOCCUS FAECALIS INFECTION. DURING HOSPITALIZATION, THE PATIENT RECEIVED AMPICILLIN.THE PATIENT'S CURRENT CHEMOTHERAPY REGIMEN INCLUDES CARBOPLATIN AND ETOPOSIDE, AND THE PATIENT IS CURRENTLY IMMUNOCOMPROMISED.OTHER MEDICATIONS THE PATIENT IS CURRENTLY TAKING ARE: SKYRIZI, DOXAZOSIN MESYLATE, FAMOTIDINE, CARVEDILOL, LOW-DOSE ASPIRIN, ACYCLOVIR, AMLODIPINE DESYLATE. THE PATIENT HAS KNOWN ALLERGIES TO IBUPROFEN AND IODINATED CONTRAST MEDIA.

  Patient problems: Bacterial Infection; Fever; Unspecified Infection

  MAUDE report 24780576 ↗
• InjuryApr 3, 2026Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED THEY THINK THEY MAY HAVE AN INFECTION BECAUSE OF THE ALCOHOL PREP. ADDITIONAL INFORMATION RECEIVED STATED THE PATIENT WAS USING THE ALCOHOL PREPS TO CLEAN HIS LEG TO START A NEW SITE FOR A REMODULIN INJECTION SUB Q. THE PATIENT'S LEG BECAME PAINFUL MORE THAN NORMAL AND SWELLED UP 3 INCHES MORE THAN NORMAL. HIS LEG HAD A 102 TEMP ON IT UNTIL HE REMOVED THE SITE AND CLEANED IT VERY WELL. THE INJECTION POINT IS STILL VERY RED, AND THE PATIENT STILL HAS PAIN. THE REDNESS ON THE REST OF THE LEG HAS STARTED TO GO AWAY. THE PAIN IS TOLERABLE NOW WHICH IS DIFFERENT THAN ANY OTHER SITE REACTION THAT THE PATIENT HAS GOTTEN FROM THE MEDICINE. THE PATIENT DID NOT SEE A DOCTOR BUT DID SPEAK TO HIS PHARMACIST. NO MEDICATIONS WERE REQUIRED.

  Patient problems: Pain; Skin Inflammation/ Irritation

  MAUDE report 24775920 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE CUSTOMER, HIS RHEUMATOID ARTHRITIS (RA) DOCTOR HAS BEEN TRYING TO FIGURE OUT WHAT¿S GOING ON. THE CUSTOMER HAD A MAJOR REACTION, BLOOD VASCULAR RASH FROM AN INFECTION, THE NIGHT AFTER TAKING HIS SHOT AND USING THE WIPE THAT WAS IN WITH ALONG WITH HIS SIMLANDI SHOT. THEN HE GOT A MESSAGE FROM HIS PHARMACY ABOUT THE WIPES. HE IS COVERED WITH A RASH THAT LOOKS LIKE LEUKOCYTOCLASTIC VASCULITIS. IT STARTED ON SAME LEG HE USED WIPE AND GAVE HIMSELF A SHOT. PER CUSTOMER, HE IS WAITING FOR ADDITIONAL TEST RESULTS.

  Patient problems: Hypersensitivity/Allergic reaction; Unspecified Infection

  MAUDE report 24772407 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED THAT SHE USES WEBCOL WIPES FOR HER WEEKLY INTRAMUSCULAR (IM) INJECTED MEDICATION AND TO CLEAN HER ELECTRIC RAZOR. SHE NOW HAS A GIANT ABSCESS, AND HER FACE IS COVERED IN SORES. SHE HAS DONE THREE ROUNDS OF DOXYCYCLINE, BUT IT ALWAYS COMES BACK.

  Patient problems: Abnormal scarring; Abscess; Dehydration; Fatigue; Swelling/ Edema; Ulcer

  MAUDE report 24772252 ↗
• InjuryApr 1, 2026Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED SHE HAS BEEN BUYING THE WEBCOL PREPS SINCE (B)(6) 2022 AND HAS HAD UNEXPLAINED MEDICAL ISSUES. SHE HAS HAD TO SEE ENDOCRINOLOGISTS, CARDIOLOGISTS, NEPHROLOGISTS, DERMATOLOGISTS, ALLERGISTS, AND MULTIPLE OTHERS. SHE HAS CHILLS, HOT FLASHES, BP ISSUES, AND REDNESS ON HER FACE AND NECK. SHE HAS USED THE PREPS ON HER FACE AND NECK AS WELL AS TO CLEAN HER PHONE, COMPUTER, AND SURFACES. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 24755405 ↗
• InjuryMar 16, 2026Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE PATIENT, SHE HAS A CONDITION OF BEING CHRONICALLY ILL. SHE WAS EXPERIENCING VOMITING FOR SEVERAL HOURS AND DIARRHEA FOR SEVERAL DAYS. SHE WAS IN AND OUT OF CONSCIOUSNESS AND COULDN'T HOLD FOOD OR WATER FOR SEVERAL DAYS. SHE CHECKED HER BLOOD PRESSURE AND NOTICED IT HAD DROPPED DANGEROUSLY LOW (84/45, 90/48, AND 60/42). CURRENTLY, SHE IS ON MEDICATION TO STABILIZE HER BLOOD PRESSURE. THE PATIENT ALSO SHOWED SYMPTOMS OF THROAT SWELLING. SHE VISITED A HEMATOLOGIST AND HER BLOOD WORK SHOWED DANGEROUSLY LOW LEVELS OF IRON (6 G/L). THE PATIENT REALIZED SHE USES CARDINAL HEALTH ALCOHOL SKIN PREP WIPES (OVER 10 TIMES A DAY) TO REGULARLY WIPE HER HANDS AND THE CENTRAL LINE ON HER MEDICAL DEVICE. THIS IS THE PROCEDURE INSTRUCTED TO HER BY MEDICAL PROFESSIONALS. SHE AT FIRST BELIEVED SHE HAD FOOD POISONING BUT THEN THOUGHT OF CALLING CARDINAL HEALTH. CARDINAL HEALTH CONFIRMED A RECENT RECALL FOR THE PADS BECAUSE OF A DISCOVERY OF TWO RESISTANT STRAINS OF BACTERIA FOUND ON SEVERAL BATCHES. SHE FURTHER STATED THAT SHE IS STILL EXPERIENCING NAUSEA, FATIGUE, NOSE BLEEDS, AND A SKIN INFECTION ON HER NOSE AND LIPS.

  Patient problems: Anemia; Decreased Appetite; Diarrhea; Epistaxis; Fatigue; Loss of consciousness; Low Blood Pressure/ Hypotension; Nausea; Skin Infection; Swelling/ Edema; Vomiting

  MAUDE report 24612704 ↗
• InjuryMar 11, 2026Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER CALLED ON (B)(6) 2026 AND LEFT A VOICEMAIL STATING THAT SHE WAS AFFECTED BY A MEDICAL RECALL OF ONE OF OUR PRODUCTS. A VOICEMAIL WAS LEFT FOR THE CUSTOMER ON 09MAR2026 AND 10MAR2026 TO REQUEST ADDITIONAL INFORMATION. THE CUSTOMER CALLED BACK ON (B)(6) 2026 AND STATED THAT SHE IS A 17-YEAR-OLD FEMALE WITH HYPERMOBILE EHLERS-DANLOS SYNDROME, GASTROPARESIS AND INTESTINAL FEVER WHICH REQUIRES A CENTRAL LINE. SHE USES WEBCOL¿ ALCOHOL PREP PADS FOR HER CENTRAL LINE CARE, SPECIFICALLY FOR DRESSING CHANGES. SHE STATED THAT SHE DID A DRESSING CHANGE ON FRIDAY, (B)(6) 2026 AND ON THE FOLLOWING DAY SHE NOTICED AN INFECTION AROUND HER LINE WHERE SHE HAD USED THE WIPES. SHE NOTED THERE TO BE PUS AROUND THE SITE. SHE WENT TO THE HOSPITAL ON SUNDAY (B)(6) 2026 AND WAS ADMITTED. SHE RECEIVED IV ANTIBIOTICS WHICH CONSISTED OF 4 DIFFERENT TYPES DUE TO ALLERGIES AND THE MEDICAL TEAM TRYING TO CLEAR THE INFECTION. THE CENTRAL LINE NEEDED TO BE SURGICALLY REMOVED AND A NEW LINE WAS PLACED ELSEWHERE IN HER BODY. SHE WAS DISCHARGED FROM THE HOSPITAL ON THURSDAY, (B)(6) 2026 WITH TAKE-HOME IV ANTIBIOTICS. ONCE HOME, SHE CONTINUED TO USE THE SAME BOX OF WEBCOL¿ ALCOHOL PREP PADS AND DEVELOPED

  Patient problems: Fatigue; Unspecified Infection

  MAUDE report 24573528 ↗
• InjuryMar 11, 2026Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER CALLED AND STATED THAT SHE HAS BEEN USING THE ALCOHOLIC WIPES THAT HAVE BEEN RECALLED AND SHE HAS BEEN IN THE HOSPITAL THE LAST FEW MONTHS FIVE TIMES FOR INFECTIONS. DURING A FOLLOW-UP CALL ON (B)(6) 2026, THE CUSTOMER REPORTED BEING IN AND OUT OF THE HOSPITAL FOR THE PAST FIVE WEEKS. THESE ISSUES BEGAN ON (B)(6) 2026, WITH SURGERY TO REMOVE A LIVER TUMOR AND THE INSERTION OF A BILIARY DRAIN TUBE WITH A BAG. TWO WEEKS LATER, A BLOCKAGE IN THE BAG RESULTED IN A SECOND SURGERY FOR REPLACEMENT. BY LATE ON (B)(6), SHE DEVELOPED A 103 DEGREE FEVER AND HER BLOOD PRESSURE DROPPED TO 50/60. THIS LED TO A THIRD SURGERY TO CHANGE THE BAG DUE TO AN INFECTION, WITH DOCTORS SUSPECTING SEPSIS. ALTHOUGH CULTURES AND BLOOD WORK WERE PERFORMED, SHE WAS UNSURE OF THE RESULTS AT THE TIME OF THE CALL BUT BELIEVED THEY WERE IN HER PORTAL, NOTING THAT THE HOSPITAL STRUGGLED TO IDENTIFY THE SOURCE OF HER RECURRING INFECTIONS. SHE HAS BEEN ON AMOXICILLIN FOR TWO MONTHS. SHE STATED THAT SHE IS A SEVEN-YEAR CANCER SURVIVOR AND IS NOW OFF CHEMOTHERAPY. SHE ALSO STATED THAT SHE STARTED USING THE ALCOHOL PREP PAD BOX SIX WEEKS AGO. SHE HAS BEEN INSERTING THE PADS INTO HER BILIARY TUBE BEFORE USING

  Patient problems: Fever; Low Blood Pressure/ Hypotension; Skin Inflammation/ Irritation; Unspecified Infection

  MAUDE report 24565953 ↗