Halyard drape packs shipped without undergoing validated sterilization process
Halyard Drape Packs, kit code LMDP36-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 72 kits affected.
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: FDA Class II recall where surgical drapes were distributed without validated sterilization, a risk of harm with no injuries reported in the source.
Plain-English summary
The Halyard Drape Pack, kit code LMDP36-01, UDI-DI 10809160479148, is being recalled. The action covers 72 kits, with an expiration date of 9/10/2028.
The stated reason is the inadvertent distribution of sealed pouches that had not undergone validated sterilization. The FDA classified the action as Class II.
Distribution was within the United States, in Iowa. The drape packs are supplied to healthcare facilities rather than sold to consumers.
Facilities should identify affected kits using the kit code, UDI-DI and expiration date above, quarantine them, and follow the instructions issued by the manufacturer.
The recalled product
- Product
- Halyard, Drape Pack. Kit Code: LMDP36-01.
- Manufacturer
- AVID Medical, Inc.
- Affected units
- 72
Distribution
Part of a larger recall action
This product is one of 4 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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