MAUDE Adverse Event Report: FISHER & PAYKEL HEALTHCARE LTD F&P SLEEPSTYLE AUTO CPAP; BZD

Model Number SPSAAJ

Device Problems Break (1069); Detachment of Device or Device Component (2907)

Patient Problem No Consequences Or Impact To Patient (2199)

Event Date 01/17/2019

Event Type  malfunction  

Manufacturer Narrative

(b)(4).The complaint f&p sleepstyle series cpap is currently en route to fisher & paykel healthcare in (b)(4) for evaluation.We will provide a follow-up report upon completion of our investigation.

Event Description

A healthcare facility in (b)(6) reported that a pin from the mains inlet socket had come apart.There was no reported patient involvement nor user consequence.

Manufacturer Narrative

(b)(4).Method: the complaint f&p sleepstyle series cpap was received at fisher & paykel healthcare in new zealand and was visually inspected internally and externally.Results: visual inspection confirmed that one pin had detached from the mains inlet socket and the second was loose.Conclusion: the reported incident was traced to an issue in the assembly process of the supplied mains inlet connector component.The supplier of the component was notified and they have made changes to the assembly process.As part of our ongoing product improvement initiatives, we recently implemented a gauge test which identifies and rejects any potentially faulty mains inlet sockets prior to assembly into the sleepstyle.The subject sleepstyle was manufactured prior to implementation of these measures.Our user instructions that accompany the f&p sleepstyle state the following: do not use if the device, power cord or accessories are damaged, deformed, or cracked.Do not pull on the power cord as it may become damaged.Turn the device off at the power supply, then remove the power cord from the rear of the device.

Event Description

A healthcare facility in japan reported that a pin from the mains inlet socket had come apart.There was no reported patient involvement nor user consequence.

• Brand Name: F&P SLEEPSTYLE AUTO CPAP
• Type of Device: BZD
• Manufacturer (Section D): FISHER & PAYKEL HEALTHCARE LTD; 15 maurice paykel place; east tamaki; auckland, 2013 ; NZ 2013
• MDR Report Key: 8346485
• MDR Text Key: 137837701
• Report Number: 9611451-2019-00123
• Device Sequence Number: 1
• Product Code: BZD
• UDI-Device Identifier: 09420012445650
• UDI-Public: (01)09420012445650(10)2100581799(11)180912
• Combination Product (y/n): N
• PMA/PMN Number: K173193
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,user facility
• Type of Report: Initial,Followup
• Report Date: 01/23/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 02/17/2019
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Lay User/Patient
• Device Model Number: SPSAAJ
• Device Catalogue Number: SPSAAJ
• Device Lot Number: 2100581799
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 03/27/2019
• Date Manufacturer Received: 04/11/2019
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1