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RecallWatchMedical Device Safety
Class IIOngoingZ-3046-2026

AVID Medical, Inc. recalls Halyard medical convenience kits labeled as: 1) A-P PACK - 205936

AVID Medical, Inc.Toano, VA, United StatesReported Sep 9, 2026 · 6 days ago
Legal News Analyst ·

Reason for recall

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.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Halyard medical convenience kits labeled as: 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 / code information

Part / Item #
(kit) ANAP22-01, UDI/DI 10809160473146, Kit
Lot #
346967; Model/
Part / Item #
(kit) ANAP22-01, UDI/DI 10809160473146, Kit
Lot #
346982; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343413; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343414; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343713; Model/
Show 50 more code fields
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343715; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343716; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343412; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343416; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343714; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343717; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343718; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343719; Model/
Part / Item #
(kit) ANPP15-01, UDI/DI 10809160473573, Kit
Lot #
343723; Model/
Part / Item #
(kit) BPAY14-01, UDI/DI 10809160473979, Kit
Lot #
343746; Model/
Part / Item #
(kit) BPAY14-01, UDI/DI 10809160473979, Kit
Lot #
343747; Model/
Part / Item #
(kit) BPAY14-01, UDI/DI 10809160473979, Kit
Lot #
343771; Model/
Part / Item #
(kit) BPAY14-01, UDI/DI 10809160473979, Kit
Lot #
374128; Model/
Part / Item #
(kit) BPAY14-01, UDI/DI 10809160473979, Kit
Lot #
374129; Model/
Part / Item #
(kit) BPAY14-01, UDI/DI 10809160473979, Kit
Lot #
374296; Model/
Part / Item #
(kit) HSLM53-01, UDI/DI 10809160476888, Kit
Lot #
342005; Model/
Part / Item #
(kit) HSLM53-01, UDI/DI 10809160476888, Kit
Lot #
344071; Model/
Part / Item #
(kit) HSLM53-01, UDI/DI 10809160476888, Kit
Lot #
347906; Model/
Part / Item #
(kit) HSLM53-01, UDI/DI 10809160476888, Kit
Lot #
341835; Model/
Part / Item #
(kit) HSLM53-01, UDI/DI 10809160476888, Kit
Lot #
343206; Model/
Part / Item #
(kit) HSLM53-01, UDI/DI 10809160476888, Kit
Lot #
343208; Model/
Part / Item #
(kit) MHAC65-01, UDI/DI 10809160479537, Kit
Lot #
345289; Model/
Part / Item #
(kit) MHSP99-01, UDI/DI 10809160479797, Kit
Lot #
345694; Model/
Part / Item #
(kit) MHSP99-01, UDI/DI 10809160479797, Kit
Lot #
341654; Model/
Part / Item #
(kit) WECR41-01, UDI/DI 10809160485392, Kit
Lot #
344464

What the firm is doing

Owens & Minor issued an URGENT: MEDICAL DEVICE RECALL NOTIFICATION to its consignees on 5/19/2026 via email. The notice explained the issue, potential risk to health and requested the following: "ACTIONS TO TAKE: " Identify, segregate, and quarantine all impacted product. " Add recall labels to affected Avid kits to ensure all users are aware of the actions to discard the impacted component. A labeling template is enclosed for printing labels which can be affixed on all affected kits and cases in inventory. Please contact your Sales Representative if pre-printed labels are needed. This label should be applied in a prominently visible location to end-users. The location chosen should not cover any other critical product information found on existing product labeling. " Customers (end-users): If you received product from a distributor, please contact the distributor or your sales representative with any questions you may have. " Distributors: If any of the affected kits identified above were further distributed, please ensure all end-users are appropriately notified and maintain records of effectiveness."

DistributionShow details

US Nationwide distribution in the states of AZ, CA, CO, WA, WY, TX, MI, FL, MD, UT, NC, MS, PA, MO, IA, NE, OH, IL, SD, MN, GA.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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