Where's it on?
FDA · Medical devices ·

Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit) recall

AVID Medical, Inc. recalled Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit) on September 23, 2026 because of potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. It was sold in IL, NC, VA, WY.

Why it was recalled

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

What's recalled

Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;

Quantity: 1640 kits

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
AVID Medical, Inc., Toano, VA
Date
Severity
Class I · most serious
the most serious: the product could cause serious health problems or death.
Where sold
IL, NC, VA, WY
Domestic: IL, NC, VA, WY;
Status
Ongoing
Recall number
Z-3151-2026
Source
U.S. Food and Drug Administration

More medical devices recalls

Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector
· Olympus Corporation of the AmericasMedline convenience kits containing Healthmark Instrument Channel Brushes
· Medline Industries, LPMidmark IQvitals Zone
· Midmark CorporationAchieva 3.0T; Model Numbers (REF)
· Philips North America LlcAutomated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1
· Abiomed, Inc.INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP, Replacement Set
· CooperSurgical, Inc.