MAUDE Adverse Event Report: C.R. BARD, INC. (BASD) -3006260740 POWERPICC SOLO CATHETER; CATHETER,INTRAVASCULAR,THERAPEUTIC,LONG-TERM GREATER THAN 30 DAYS

Model Number	N/A
Medical Device Problem Code	Material Deformation (2976)
Health Effect - Clinical Code	Unspecified Tissue Injury (4559)
Date of Event	04/10/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
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.The manufacturer has received the sample and is pending evaluation.Results are expected soon.
Event or Problem Description
It was reported by the customer that the introducer will not insert into vasculature.Date of event (b)(6) 2023.Additional info received on 14-april-2023 customer reported they had to drop another introducer kit to access the patient.The event caused trauma to the skin and vessel upon insertion but did not require treatment.There was no patient harm or negative outcome.The event did not involve an urgent or life-threatening medical situation.
Event or Problem Description
It was reported by the customer that the introducer will not insert into vasculature.Date of event (b)(6) 2023.Additional info received on (b)(6) 2023 customer reported they had to drop another introducer kit to access the patient.The event caused trauma to the skin and vessel upon insertion but did not require treatment.There was no patient harm or negative outcome.The event did not involve an urgent or life-threatening medical situation.
Additional Manufacturer Narrative
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.The complaint of a difficult insertion is confirmed but the exact cause remains unknown.One 5 fr x 7 cm microez microintroducer was returned for evaluation.A product label indicating lot: regz0186 and a date, "(b)(6) 23", was written on plastic.The dilator was present within the sheath which had not been peeled.The sheath and shaft appeared to be slightly bent.Blood residue and evidence of use was noted on the device.One photo sample of a microez microintroducer within a plastic bag was also provided for evaluation.The date ¿4/10/23¿ was written on the plastic bag and corresponded with the returned physical sample.Microscopic inspection of the sheath tip did not reveal any significant damage or deformation.Based on the information provided, possible contributing factors include advancement against resistance, inadequate skin incision, and sheath tip transition.The presence of a bend in the shaft suggest that a difficult insertion may have been experienced; therefore, the complaint is confirmed.H3 other text : evaluation findings are in section h.11.

• Brand Name: POWERPICC SOLO CATHETER
• Common Device Name: CATHETER,INTRAVASCULAR,THERAPEUTIC,LONG-TERM GREATER THAN 30 DAYS
• Manufacturer (Section D): C.R. BARD, INC. (BASD) -3006260740; 605 north 5600 west; salt lake city 84116
• Manufacturer (Section G): BARD REYNOSA S.A. DE C.V. -9617592; blvd. montebello #1; parque industrial colonial; reynosa, tamaulipas 88780 ; MX 88780
• Manufacturer Contact: becky garcia ; 605 north 5600 west; salt lake city 84116 ; 8015950700
• MDR Report Key: 16820399
• Report Number: 3006260740-2023-01551
• Device Sequence Number: 20615932
• Product Code: LJS
• UDI-Device Identifier: 00801741223938
• UDI-Public: (01)00801741223938
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• PMA/510(K) Number: UNK
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 05/15/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 04/30/2024
• Device Model Number: N/A
• Device Catalogue Number: CK001028
• Device Lot Number: REGZ0186
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/14/2023
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 04/11/2023
• Supplement Date Received by Manufacturer: 05/15/2023
• Initial Report FDA Received Date: 04/26/2023
• Supplement Report FDA Received Date: 05/18/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 12/01/2022
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown