Pd-l1 Ihc 22c3 Pharmdx
PD-L1 IHC 22C3 pharmDx Recall Agilent Technologies is recalling the PD-L1 IHC 22C3 pharmDx diagnostic device across Canada due to a labeling or packaging defect. This is a Class II recall, meaning the product could cause temporary health problems or pose a potential health hazard. The defect affects the labeling or packaging on the product.
- Recalling firm
- Agilent Technologies, Inc.
- Product
- PD-L1 IHC 22C3 pharmDx
- Reason
- Labelling or packaging defect
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-10-28
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/72865758-7f9d-489b-8a25-500eb2c96f76