DP-30 Digital Ultrasonic Diagnostic Imaging System, Part No. 1155E-PA00004 - Product Usage: The Digital Ultrasonic Diagn
FDA device recall Z-1330-2020 · posted 2020-02-05 · Terminated
Recall details
- Recalling firm
- Mindray DS USA, Inc. dba Mindray North America
- Reason for recall
- The DP-30 displays an incorrect needle-guide bracket when used with the 65EC10EA model transducer.
- Action taken
- On January 13, 2020, the firm distributed Urgent Medical Device Correction letters to affected distributors. Distributors were informed that the system displays the incorrect needle-guide bracket when used with the 65EC10EA model transducer. Customers were advised to avoid use of NGB-004 needle-guide with transducer model 65EC10EA until a software update has been applied to the system. The system may be used normally for all other functions. The firm recommended that distributors immediately notify any clients to which they have distributed affected systems (DP-30 systems with software version 03.00.00 and 03.01.00 distributed between 06/25/2018 and 06/28/2019), or provided a software update (USB with V03.01.00, part number 110-002261-05). Within the next several weeks, Mindray will provide a software update at no cost. Should you require technical assistance while performing the update, please contact Mindrays Technical Support team at 800-288-2121, option 2, Monday through Friday, 8:30am - 5:30pm PT. The replacement USB drive contains instructions on how to perform the software update, under the Manuals folder in the DP-10 & DP-20 & DP-30 Series System Recovery Guide file. If you have questions regarding this recall, you may contact Diane Arpino, Director, Quality Operations and Regulatory Affairs, at 201-995-8407, or via email at d.arpino@mindray.com.
- Root cause
- Software Design Change
- Status
- Terminated
- Product code
- IYN
- Quantity affected
- 53 DP-30 systems and 18 USB's containing the affected software
- Distribution
- US Nationwide distribution in the states of CA, GA, IL, MD, NY, SC, and WA.
- Date initiated
- 2020-01-13
- Date posted
- 2020-02-05
- Date terminated
- 2020-08-21
- Location
- Mahwah, NJ
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| DP-10/DP-20/DP-30 Digital Ultrasonic Diagnostic Imaging System (K183660) | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 2019-04-09 |