PlainRecalls
FDA Devices Moderate Class II Ongoing

Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.

Reported: December 24, 2025 Initiated: November 14, 2025 #Z-0929-2026

Product Description

Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.

Reason for Recall

Potential for incomplete seal on header bag.

Details

Recalling Firm
AVID Medical, Inc.
Units Affected
90 units
Distribution
US distribution to GA, IL, NE, MD.
Location
Toano, VA

Frequently Asked Questions

What product was recalled?
Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.. Recalled by AVID Medical, Inc.. Units affected: 90 units.
Why was this product recalled?
Potential for incomplete seal on header bag.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 24, 2025. Severity: Moderate. Recall number: Z-0929-2026.