- Recalling firm
- AVID Medical, Inc.
- Reason for recall
- Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
- Affected products (lot / model / serial)
- Model/Item Number (Kit): DPGE002-02; UDI-DI: 10809160410325; Kit Lots: 1641713, 1641714, 1659697, 1668209; Recalled Sodium Chloride Ampule Lot: AB4003;
- Units affected
- 1640 kits
- Distribution pattern
- Domestic: IL, NC, VA, WY;
- Firm location
- Toano, VA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3151-2026
- Recall initiated
- August 10, 2026
- FDA classification date
- September 16, 2026
- FDA report date
- September 23, 2026
- FDA event ID
- 99758
- Last updated on HTM Vibe
- September 29, 2026