Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868
Lot Codes / Batch Numbers
Lot Numbers: 070494, 070548, 070551, 070481, 070490, 070495, 070542, 070496
Products Sold
Lot Numbers: 070494, 070548, 070551, 070481, 070490, 070495, 070542, 070496
A medical device manufacturer is recalling Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868 due to The firm has become aware that the Snapshot Trackers were not manufactured in accordance with specifications and could potentially lead to navigation. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm has become aware that the Snapshot Trackers were not manufactured in accordance with specifications and could potentially lead to navigational inaccuracies, which may result in patient injury, e.g. nerve damage or neurological deficit/dysfunction
Recommended Action
Per FDA guidance
On 07/05/2019, a "Urgent: Medical Device Recall" notification letter was hand-delivered to affected customers. In addition to informing consignees about the recall, the letter also asked customers to take the following actions: 1. Your Medtronic representative will be visiting you to remove the affected Tracker(s) and provide you with replacement Tracker(s). 2. Please sign the Consignee Confirmation Form accompanying this notification, acknowledging that you have reviewed this information as well as received a replacement product, and please return it to your Medtronic representative. 3.Adverse events or quality problems experienced with this product should be reported to FDA and Medtronic: - Online at the FDA website (www.fda.gov) or call FDA at 1-800-FDA-1088. - E-mail Medtronic at rs.navtechsupport@medtronic.com or call 1-888-826-5603. 4. If you have any questions regarding this communication, please contact Medtronic at 1-888-826-5603.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, AR, CA, CO, CT, FL, GA, IL, IN, KY, LA, MD, MA, MI, MN, NY, NC, ND, PA, SC, SD, TN, TX, UT, VA, WV
Page updated: Jan 10, 2026