Halyard recall
Halyard, Drape Pack. Kit Code: LMDP36-01.
Why was Halyard recalled?
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028
- Product
- Halyard, Drape Pack. Kit Code: LMDP36-01.
- Recalling firm
- AVID Medical, Inc.
- Quantity
- 72 kits
- Distribution
- US Nationwide distribution in the state of Iowa.
- Recall date
- June 17, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)