- Recalling firm
- ARROW INTERNATIONAL, LLC
- Reason for recall
- Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
- Affected products (lot / model / serial)
- Product code:ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 Batch Number: 33F25K0130
- Units affected
- 115
- Distribution pattern
- U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.
- Firm location
- Morrisville, NC, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1912-2026
- Recall initiated
- March 11, 2026
- FDA classification date
- April 22, 2026
- FDA report date
- April 29, 2026
- FDA event ID
- 98618
- Last updated on HTM Vibe
- July 24, 2026