Z-1231-2017 Class II Terminated
FDA device recall Z-1231-2017 was initiated by Quidel Corporation on January 25, 2017 and is designated Class II. Reason for recall: Quidel Corporation is recalling Influenza Transport Swab Packages because it may include an incorrect sample swab mixed in with the proper swabs. The recall status is terminated (terminated June 2, 2017). Affected quantity: 1,010 packages.
Recall Details
- Product Type
- Devices
- Report Date
- March 1, 2017
- Initiation Date
- January 25, 2017
- Termination Date
- June 2, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,010 packages
Product Description
Influenza Transport Swab Packages, Reference #20171, One lot with 1010 packages (each package contains 25 transport tubes). The Influenza Swabs in dry transport tubes are intended for use with influenza tests
Reason for Recall
Quidel Corporation is recalling Influenza Transport Swab Packages because it may include an incorrect sample swab mixed in with the proper swabs.
Distribution Pattern
Nationwide Distribution to FL, GA, IL, IN, KY, MT, OH, PA, TX
Code Information
PS10171