Recall Z-3151-2026— AVID Medical, Inc.
Class I · Ongoing
Class I FDA medical device recall by AVID Medical, Inc., initiated 2026-08-10. FDA's recall record names no specific 510(k) clearance for this event. Product: Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;. Reason: Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical..
- Recalling firm
- AVID Medical, Inc.
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2026-08-10
- Firm location
- Toano, VA, United States
Product description
Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;
Reason for recall
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Data sourced from openFDA. This site is unofficial and independent of the FDA.