Official recall record
Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit) ACEN89-02; 3)
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-05-19
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 10809160459447
- Brand on record
- AVID Medical, Inc.
- Product category
- Medical Device
What the authority reported
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-10-01.
Record last checked against the registry on 2026-10-01.
Other recalls from this brand
All 48 official recall notices naming AVID Medical, Inc. on this site →
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