MAUDE Adverse Event Report: C.R. BARD, INC. (COVINGTON) -1018233 PUREWICK FEMALE EXTERNAL CATHETER

Catalog Number PWFX30

Device Problems Patient-Device Incompatibility (2682); Biocompatibility (2886)

Patient Problems Unspecified Infection (1930); Burning Sensation (2146); Patient Problem/Medical Problem (2688)

Event Type  Injury  

Manufacturer Narrative

The investigation is still in progress.Once the investigation is complete a supplemental report will be filed.The device was not returned.

Event Description

It was reported that the patient thinks the wicks gave her an infection because when she uses it, it burns when she urinates and was sore; she said she had not discussed this with her doctor and also said that she had nylon allergies and she¿s not sure if that¿s related.

Manufacturer Narrative

The reported event was inconclusive as no sample was returned for evaluation.However, the potential root for this failure could be that material surface is rough, abrasive or uncomfortable.The lot number is unknown; therefore, the device history record could not be reviewed.The instructions for use were found adequate and state the following: "contraindications: -patients with urinary retention warnings: -never insert the purewick female external catheter into vagina, anal canal or other body cavities.For external use only.-do not use purewick female external catheter with bedpan or any material that does not allow for sufficient airflow.-to avoid potential skin injury, never push or pull the purewick female external catheter against the skin during placement or removal.-discontinue use if an allergic reaction occurs.-reuse and/or repackaging may create a risk of patient or use infection, compromise the structural integrity and/or essential material and design characteristics of the device which may lead to device failure, and/or lead to injury or illness of the patient.-after use, this product may be a potential biohazard.Dispose of in accordance with applicable local, state and federal laws and regulations.Precautions: -not recommended for patients who are: -agitated, combative or unconperative and might removw the purewick female external catheter.-having frequent episodes of bowel incontinence without a fecal management system in place.-experiencing skin irritation or breakdown at the site -experiencing moderate/heavy menstruation and cannot use a tampon.-do not use barrier cream on the perineum when using the purewick female external catheter.Barrier cream may impede suction -not recommended for use on patients who have undergone recent surgery of the external urogenital tract.-always assess skin for compromise nd perform perineal care prior to placement of a new purewick female external catheter.-maintain suction until the purewick female external catheter is fully removed from he patient to avoid urine backflow.Recommendations: -perform each step with clean technique.N the home setting, wash hands thoroughly before device placement.-prior to connecting the purewick female external catheter to hospital wall suction tubing, verify suction function by covering the open end of the suction tubing with one hand and observing the pressure dial.If the pressure does not increase when the line is covered, verify that the tubing is secured, connected and not kinked.-ensure the purewick female external catheter remains in the correct position after turning the patient.Remove the purewick female external catheter prior to ambulation.-properly placing the purewick female external catheter snugly between the labia and gluteus holds the purewick female external catheter in place for most patients.Mesh underwear may be useful for securing the purewick female external catheter for some patients.-assess device placement and patient's skin at least every 2 hours.-replace the purewick female external catheter every 8-12 hours or when soiled with feces or blood.-if using wall suction, change suction tubing per hospital protocol or at least every thirty (30) days.-if using purewick urine collection system, replace accessories per purewick urine collection system user guide." h11:section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.H3 other text : the device was not returned.

Event Description

It was reported that the patient thinks the wicks gave her an infection because when she uses it, it burns when she urinates and was sore; she said she had not discussed this with her doctor.She said she had nylon allergies and she¿s not sure if that¿s related.

• Brand Name: PUREWICK FEMALE EXTERNAL CATHETER
• Type of Device: PUREWICK FEMALE EXTERNAL
• Manufacturer (Section D): C.R. BARD, INC. (COVINGTON) -1018233; 8195 industrial blvd; covington GA 30014
• MDR Report Key: 10046477
• MDR Text Key: 190605745
• Report Number: 1018233-2020-03134
• Device Sequence Number: 1
• Product Code: NZU
• UDI-Device Identifier: 00801741189050
• UDI-Public: (01)00801741189050
• Combination Product (y/n): N
• PMA/PMN Number: EXEMPT
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: consumer,distributor,other
• Type of Report: Initial,Followup
• Report Date: 05/27/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 05/12/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Lay User/Patient
• Device Catalogue Number: PWFX30
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 05/19/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Other