Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIOngoing
Summary: AVID Medical, Inc. is recalling Halyard, Drape Pack. Kit Code: LMDP36-01.. Reason: Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
What is being recalled
Halyard, Drape Pack. Kit Code: LMDP36-01.
Why
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the state of Iowa. (states named: Iowa)
How to tell if yours is affected
Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2409-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | April 30, 2026 |
| Reported | June 17, 2026 |
| Company | AVID Medical, Inc. |
| Company location | Toano, VA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 72 kits |
More recalls from AVID Medical, Inc. · all medical device recalls · recalls from April 2026