Reported Sep 9, 2026 · Ongoing · Updated Sep 16, 2026
Halyard medical convenience kits labeled as
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?
Halyard medical convenience kits labeled as
53 of 53 products
| # | Product as published |
|---|---|
| 1 | ENT, Model/Item Number (kit) ACEN89-01 |
| 2 | ENT, Model/Item Number (kit) ACEN89-02 |
| 3 | BACK PACK, Model/Item Number (kit) ALBK51-01 |
| 4 | DR DERIAN SPINE PACK SNEDHCPDH, Model/Item Number (kit) DGSP71 |
| 5 | BASIC PACK DR BROWN SBADHBPR16, Model/Item Number (kit) DRBS37 |
| 6 | BASIC PACK DR BROWN SBADHBPR16, Model/Item Number (kit) DRBS37-01 |
| 7 | NASAL PACK SEN23SNRC3, Model/Item Number (kit) DRNS92 |
| 8 | NASAL PACK SEN23SNRC3, Model/Item Number (kit) DRNS92-01 |
| 9 | NASAL PACK SEN23SNRC3, Model/Item Number (kit) DRNS92-02 |
| 10 | SPINE PACK DR BROWN SNEDHSPR14, Model/Item Number (kit) DRSP26 |
| 11 | SPINE PACK DR BROWN SNEDHSPR14, Model/Item Number (kit) DRSP26-01 |
| 12 | SPINE PACK DR BROWN SNEDHSPR14, Model/Item Number (kit) DRSP26-02 |
| 13 | SPINE DR HEYS PACK SNE23SSRCT, Model/Item Number (kit) DRSP52 |
| 14 | SPINE DR HEYS PACK SNE23SSRCT, Model/Item Number (kit) DRSP52-01 |
| 15 | OHN LARYNGOSCOPY PACK SEN23BRD, Model/Item Number (kit) DULY32 |
| 16 | OHN LARYNGOSCOPY PACK SEN23BRD, Model/Item Number (kit) DULY32-01 |
| 17 | MICRO FLAP PK SEN23EN14T, Model/Item Number (kit) DUMF13-01 |
| 18 | MICRO FLAP PK SEN23EN14T, Model/Item Number (kit) DUMF13-02 |
| 19 | OHN NASAL PROCEDURE PACK SEN23, Model/Item Number (kit) DUNS94 |
| 20 | OHN NASAL PROCEDURE PACK SEN23, Model/Item Number (kit) DUNS94-01 |
- Lot codes and dates
168 of 168 products
Products covered by this recall # Barcodes Product as published 1 10809160459447Model/Item Number (kit) ACEN89-01, UDI/DI 10809160459447, Kit Lot Number 1650691 2 10809160496411Model/Item Number (kit) ACEN89-01, UDI/DI 10809160496411, Kit Lot Number 1675577 3 10809160459447Model/Item Number (kit) ACEN89-01, UDI/DI 10809160459447, Kit Lot Number 1666553 4 10809160505304Model/Item Number (kit) ACEN89-02, UDI/DI 10809160505304, Kit Lot Number 1683926 5 10809160505304Model/Item Number (kit) ACEN89-02, UDI/DI 10809160505304, Kit Lot Number 1683927 6 10809160458587Model/Item Number (kit) ALBK51-01, UDI/DI 10809160458587, Kit Lot Number 1649240 7 10809160458587Model/Item Number (kit) ALBK51-01, UDI/DI 10809160458587, Kit Lot Number 1649721 8 10809160496374Model/Item Number (kit) ALBK51-01, UDI/DI 10809160496374, Kit Lot Number 1675589 9 10809160468036Model/Item Number (kit) DGSP71, UDI/DI 10809160468036, Kit Lot Number 1659332 10 10809160466858Model/Item Number (kit) DRBS37, UDI/DI 10809160466858, Kit Lot Number 1658530 11 10809160503829Model/Item Number (kit) DRBS37-01, UDI/DI 10809160503829, Kit Lot Number 1681363 12 10809160503829Model/Item Number (kit) DRBS37-01, UDI/DI 10809160503829, Kit Lot Number 1681470 13 10809160503829Model/Item Number (kit) DRBS37-01, UDI/DI 10809160503829, Kit Lot Number 1691461 14 10809160466346Model/Item Number (kit) DRNS92, UDI/DI 10809160466346, Kit Lot Number 1658536 15 10809160503942Model/Item Number (kit) DRNS92-01, UDI/DI 10809160503942, Kit Lot Number 1681504 16 10809160509463Model/Item Number (kit) DRNS92-02, UDI/DI 10809160509463, Kit Lot Number 1696890 17 10809160466384Model/Item Number (kit) DRSP26, UDI/DI 10809160466384, Kit Lot Number 1659340 18 10809160505113Model/Item Number (kit) DRSP26-01, UDI/DI 10809160505113, Kit Lot Number 1683469 19 10809160509470Model/Item Number (kit) DRSP26-02, UDI/DI 10809160509470, Kit Lot Number 1691780 20 10809160466391Model/Item Number (kit) DRSP52, UDI/DI 10809160466391, Kit Lot Number 1658538 - Amount recalled
- 11763 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.
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