Reported Sep 9, 2026 · Ongoing · Updated Sep 16, 2026
1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3) CRANI, (kit) AKCR19-01; 4) ORTHO SPINE PACK, (kit) ARMC017; 5)…
AVID Medical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: AVID Medical, Inc. · 9000 Westmont Dr · Toano, VA · 23168-9351
Is this the product you have?
71 of 71 products
| # | Product as published |
|---|---|
| 1 | NEURO, (kit) ACNE73-01 |
| 2 | NEURO, (kit) ACNE73-03 |
| 3 | CRANI, (kit) AKCR19-01 |
| 4 | ORTHO SPINE PACK, (kit) ARMC017 |
| 5 | BMHM NEURO PACK, (kit) BMHT016-05 |
| 6 | LUMBAR PACK, (kit) BMHT112-03 |
| 7 | NEURO LAMINECTOMY PACK, (kit) DGNE75 |
| 8 | NEURO LAMINECTOMY PACK, (kit) DGNE75-02 |
| 9 | DRAH NEURO LAMINECTOMY SNEDHDN,(kit) DRNE75 |
| 10 | DRAH NEURO LAMINECTOMY SNEDHDN, (kit) DRNE75-01 |
| 11 | CRANIOSYNOSTOSIS CUSTOM SNE23C, (kit) DUCR36-01 |
| 12 | CRANIOSYNOSTOSIS CUSTOM SNE23C, (kit) DUCR36-02 |
| 13 | NEURO CRANIOTOMY PK SNE23C1116, (kit) DUNC42-01 |
| 14 | PEDS NEURO PACK SNE2301147, (kit) DUNE88-01 |
| 15 | NEURO SPINE PACK SNE23LM110, (kit) DUSP98-01 |
| 16 | NEURO SPINE PACK SNE23LM110, (kit) DUSP98-02 |
| 17 | CRANI PACK 712638, (kit) EFCR86-01 |
| 18 | SPINE PACK 712040, (kit) EFSP30-01 |
| 19 | SPINE PACK 712040, (kit) EFSP30-02 |
| 20 | CRANIOTOMY TRAY, (kit) EURO009-09 |
- Lot codes and dates
201 of 201 products
Products covered by this recall # Barcodes Product as published 1 10809160458532Model/Item Number (kit) ACNE73-01, UDI/DI 10809160458532, Kit Lot Number 1649716 2 10809160458532Model/Item Number (kit) ACNE73-01, UDI/DI 10809160458532, Kit Lot Number 1666559 3 10809160458532Model/Item Number (kit) ACNE73-01, UDI/DI 10809160458532, Kit Lot Number 1649717 4 10809160513996Model/Item Number (kit) ACNE73-03, UDI/DI 10809160513996, Kit Lot Number 1696563 5 10809160459515Model/Item Number (kit) AKCR19-01, UDI/DI 10809160459515, Kit Lot Number 1650945 6 10809160459515Model/Item Number (kit) AKCR19-01, UDI/DI 10809160459515, Kit Lot Number 1666564 7 10809160459515Model/Item Number (kit) AKCR19-01, UDI/DI 10809160459515, Kit Lot Number 1664544 8 10809160459515Model/Item Number (kit) AKCR19-01, UDI/DI 10809160459515, Kit Lot Number 1666978 9 10809160506455Model/Item Number (kit) ARMC017, UDI/DI 10809160506455, Kit Lot Number 1685117 10 10809160506455Model/Item Number (kit) ARMC017, UDI/DI 10809160506455, Kit Lot Number 1688043 11 10809160506455Model/Item Number (kit) ARMC017, UDI/DI 10809160506455, Kit Lot Number 1688044 12 10809160468821Model/Item Number (kit) BMHT016-05, UDI/DI 10809160468821, Kit Lot Number 1666733 13 10809160468821Model/Item Number (kit) BMHT016-05, UDI/DI 10809160468821, Kit Lot Number 1659950 14 10809160457634Model/Item Number (kit) BMHT112-03, UDI/DI 10809160457634, Kit Lot Number 1649141 15 10809160404430Model/Item Number (kit) BMHT112-03, UDI/DI 10809160404430, Kit Lot Number 1606455 16 10809160468104Model/Item Number (kit) DGNE75, UDI/DI 10809160468104, Kit Lot Number 1659330 17 10809160510001Model/Item Number (kit) DGNE75-02, UDI/DI 10809160510001, Kit Lot Number 1688056 18 10809160467190Model/Item Number (kit) DRNE75, UDI/DI 10809160467190, Kit Lot Number 1658535 19 10809160503843Model/Item Number (kit) DRNE75-01, UDI/DI 10809160503843, Kit Lot Number 1681499 20 10809160503843Model/Item Number (kit) DRNE75-01, UDI/DI 10809160503843, Kit Lot Number 1691081 - Amount recalled
- 16223 kits
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new AVID Medical, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.