FDA recall record

Agilent Technologies Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF recall — FDA Z-1384-2022

Label provided for substrate vail contained incorrect expiration date.

Class IIIclassification
Z-1384-2022official record ID
Jul 20, 2022report date

Recall record at a glance

Official recordZ-1384-2022
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmAgilent Technologies, Inc.
Report dateJul 20, 2022
Recall initiation dateMay 20, 2022
Quantity63 kits
LocationSanta Clara, CA, United States

Official 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

Why the product was recalled

Label provided for substrate vail contained incorrect expiration date.

Distribution information

U.S. Nationwide distribution in the states of NY and VA.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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