Head and neck procedure trays recalled over a potentially incomplete seal
AVID Medical is recalling 56 Halyard Head and Neck Trays over the potential for an incomplete seal on the header bag.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Scored 3 under the risk-of-harm criterion: an incomplete package seal affects the sterile barrier of a procedure tray, and no injuries are reported.
Plain-English summary
The Halyard HEAD AND NECK TRAY, catalog number EURO016-09, is being recalled by AVID Medical, Inc.
The reason given in the enforcement record is the potential for an incomplete seal on the header bag.
The record lists 56 units carrying UDI-DI 10809160461198, from lot 1655501 with an expiration of 3/31/2027. Distribution was in Georgia, Illinois, Nebraska and Maryland. The FDA has classified the action as Class II.
An incomplete seal on the packaging affects the sterile barrier of a procedure tray. The enforcement record reports no injuries. Facilities should quarantine the affected lot and follow the firm's instructions.
The recalled product
- Product
- Halyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09.
- Manufacturer
- AVID Medical, Inc.
- Category
- Medical Device — Procedure tray
- Affected units
- 56
Distribution
Part of a larger recall action
This product is one of 5 recalled by AVID Medical, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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