Z-1627-2022 Class II Ongoing

Recalled by Mckesson Medical-Surgical Inc. Corporate Office — Richmond, VA

FDA device recall Z-1627-2022 was initiated by Mckesson Medical-Surgical Inc. Corporate Office on May 25, 2022 and is designated Class II. Reason for recall: XXX The recall status is ongoing. Affected quantity: 25 Boxes.

Recall Details

Product Type
Devices
Report Date
Aug 31, 2022
Initiation Date
May 25, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
25 Boxes

Product Description

FISHER SCIENTIFIC Fisherbrand SWAB TRANS STUARTS DBL 50BX Catalog #1490721

Reason for Recall

XXX

Distribution Pattern

US Nationwide

Code Information

Unknown

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-1627-2022
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 26, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.