MAUDE Adverse Event Report: DAVOL INC., SUB. C.R. BARD, INC. SIMPULSE VARICARE SUCTION IRRIGATOR; LAVAGE, JET

Catalog Number	0067010
Medical Device Problem Codes	Break (1069); Crack (1135)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The subject product was received for evaluation.Visual evaluation found the device had been physically damaged.A crack was identified in the housing and the two halves of the housing were slightly separated from the weld.The battery pack was within the handle and the latch was noted to be broken off.The battery pack was firmly within the device.A review of the manufacturing records was performed and found that the lot was manufactured to specification.Originally the customer did not report any damage to the simpulse devices; however, after follow up with the customer, it was noted that one simpulse devices had been cracked in use.The customer contact reported that there is a possibility that these devices may be reused and the batteries may be removed and/or replaced by the user facilities.It is most likely the damage to the device occurred due to customer handling.
Event or Problem Description
It was reported per the user facility that during use of the simpulse varicare irrigator, the device would not irrigate.There was no patient injury reported.The subject product was returned and during visual inspection it was noted that the battery case latch tab was broken and not returned with the product.

• Brand Name: SIMPULSE VARICARE SUCTION IRRIGATOR
• Common Device Name: LAVAGE, JET
• Manufacturer (Section D): DAVOL INC., SUB. C.R. BARD, INC.; 100 crossings blvd.; warwick RI 02886
• MDR Report Key: 9194253
• Report Number: 1213643-2019-09969
• Device Sequence Number: 1879267
• Product Code: FQH
• UDI-Device Identifier: 00801741065293
• UDI-Public: (01)00801741065293
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: K942886
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: distributor,user facility
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 10/15/2019

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: 10/28/2021
• Device Catalogue Number: 0067010
• Device Lot Number: JUCYF194
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 09/27/2019
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/27/2019
• Initial Report FDA Received Date: 10/15/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1