Recall Z-1384-2022— Agilent Technologies, Inc.
Class III · Ongoing
Class III FDA medical device recall by Agilent Technologies, Inc., initiated 2022-05-20. FDA's recall record names no specific 510(k) clearance for this event. Product: Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-21 Vial Labels: Mat. No K589911-21512. Reason: Label provided for substrate vail contained incorrect expiration date..
- Recalling firm
- Agilent Technologies, Inc.
- Classification
- Class III
- Status
- Ongoing
- Initiated
- 2022-05-20
- Firm location
- Santa Clara, CA, United States
Product description
Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-21 Vial Labels: Mat. No K589911-21512
Reason for recall
Label provided for substrate vail contained incorrect expiration date.
Data sourced from openFDA. This site is unofficial and independent of the FDA.