Reported Sep 9, 2026 · Ongoing · Updated Sep 14, 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
7 of 7 products
| # | Product as published |
|---|---|
| 1 | A-P PACK - 205936, Model/Item Number (kit) ANAP22-01 |
| 2 | POSTERIOR PACK - 205960, Model/Item Number (kit) ANPP15-01 |
| 3 | ANEURYSM PACK, Model/Item Number (kit) BPAY14-01 |
| 4 | SPINE PACK, Model/Item Number (kit) HSLM53-01 |
| 5 | ANTERIOR CERVICAL PACK - 205988, Model/Item Number (kit) MHAC65-01 |
| 6 | SPINE PACK - 206013, Model/Item Number (kit) MHSP99-01 |
| 7 | CRANI PACK, Model/Item Number (kit) WECR41-01. |
- Lot codes and dates
30 of 30 products
Products covered by this recall # Barcodes Product as published 1 10809160473146Model/Item Number (kit) ANAP22-01, UDI/DI 10809160473146, Kit Lot Number 346967 2 10809160473146Model/Item Number (kit) ANAP22-01, UDI/DI 10809160473146, Kit Lot Number 346982 3 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343413 4 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343414 5 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343713 6 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343715 7 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343716 8 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343412 9 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343416 10 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343714 11 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343717 12 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343718 13 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343719 14 10809160473573Model/Item Number (kit) ANPP15-01, UDI/DI 10809160473573, Kit Lot Number 343723 15 10809160473979Model/Item Number (kit) BPAY14-01, UDI/DI 10809160473979, Kit Lot Number 343746 16 10809160473979Model/Item Number (kit) BPAY14-01, UDI/DI 10809160473979, Kit Lot Number 343747 17 10809160473979Model/Item Number (kit) BPAY14-01, UDI/DI 10809160473979, Kit Lot Number 343771 18 10809160473979Model/Item Number (kit) BPAY14-01, UDI/DI 10809160473979, Kit Lot Number 374128 19 10809160473979Model/Item Number (kit) BPAY14-01, UDI/DI 10809160473979, Kit Lot Number 374129 20 10809160473979Model/Item Number (kit) BPAY14-01, UDI/DI 10809160473979, Kit Lot Number 374296 - Amount recalled
- 816 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.
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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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