FDA Recall
Open, Classified
Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider, Nano-Coated, Compatible w/ FT10 37 cm FT10 SW Version 4.0.1.15 or lower. Item Number: LF1937CR.
Recall: Z-3093-2024
·
Initiated May 7, 2024
Recall
- Recall Number
- Z-3093-2024
- Event Number
- 95126
- Firm
- MEDLINE INDUSTRIES, LP Northfield
- FEI Number
- 1417592
- Product Code
- NUJ
- Status
- Open, Classified
- Root Cause
- Under Investigation by firm
- Initiated
- May 7, 2024
- Posted
- September 10, 2024
- Address
- 3 Lakes Dr, Northfield, IL, 60093-2753
Description
Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider, Nano-Coated, Compatible w/ FT10 37 cm FT10 SW Version 4.0.1.15 or lower. Item Number: LF1937CR.
Reason
Potential for an incomplete seal on the packaging tray.
Action
Medline notified consignees on about 05/06/2024 via letter sent email or First-Class mail. Consignees were instructed to examine inventory and quarantine any affected units, return any affected product that they may have on hand for credit or replacement, notify customers or personnel if the affected product was further distributed or transferred, and complete and return the response form.
Distribution
US Nationwide distribution.
Quantity
2,860 units