FDA Medical Device Recalls (openFDA)
AGILENT TECHNOLOGIES INC./US: Agilent Resolution ctDx FIRST Sample Collection Kit, 500032
- Recall number
- Z-1358-2023
- Recalling firm
- AGILENT TECHNOLOGIES INC./US
- Product
- Agilent Resolution ctDx FIRST Sample Collection Kit, 500032
- Status
- Open, Classified
- Initiated
- 2023-02-17
- Posted
- 2023-04-11
- Terminated
- not on file
- Reason
- Distributed sample collection kit with an unapproved instruction for use.
- Root cause
- Labeling Change Control
- Action
- On 02/17/2023, the firm verbally notified its customers that as part of their post-approval commitments to FDA, a final version of the product labeling was submitted to FDA on 01/17/2023. Upon FDA's review of the final label version, FDA deemed the Instruction For Use changes to be significant, such as, changes to allow use of an alternate form to document patient information and modified shipping instructions. On or about 03/23/2023, a formal updated "URGENT: Medical Device Recall" letter will be communicated to customer providing them with the recall details. Customers are instructed to: 1. Stop use of Sample Collection Kits and place under quarantine (see Table 1 for affected product and lot numbers). 2. Complete the following four (4) records and return them to Resolution s Quality Team at qa.pdl-resolution@agilent.com: i. Attachment 1, Recall Acknowledgement and Customer Return Form: Confirm that you have received this notification by returning enclosed acknowledgement form within 3 business days of receipt, answering the questions, documenting the inventory quantities, and completing the acknowledgement box. ii. Prepare the inventory for return according to provided instructions in Attachment 2, Shipping Instructions iii. Attachment 3, Product Return - Shipping Record: For each lot number and Quest Hub location, record the number of unused products being returned, shipped by and date, shipping tracking number, scan attachment 3 and email to qa.pdl-resolution@agilent.com, include attachment 3 with the shipment. iv. Attachment 4, Certification of Product Destruction Record: If there are any devices that were opened or in the process of being used please document their destruction in this attachment, scan and return via email to qa.pdl-resolution@agilent.com. Destroy devices following your laboratory procedures as deemed appropriate by your company. For questions, contact Agilent Corporate Communications at 669-225-7696 or via emails at sarah.litton@agilent.co
- Quantity
- 560 kits
- Distribution
- U.S. Nationwide distribution in the states of CA, GA, IN, NJ, and TX. O.U.S.: None
- Lot, serial or model codes
- Model/Part Number: 50032 UDI Code: N/A, single site PMA Lot Numbers: 23-0139 23-0140 23-0142 23-0143 23-0159
- 510(k) numbers
- not on file
- PMA numbers
- ["P210040","P210040/A005","P210040/A006"]
- Product code
- PQP
- Firm FEI
- 3019893001
- Firm city
- Kirkland
- Firm state
- WA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28