Z-1091-2018 Class II Terminated
FDA device recall Z-1091-2018 was initiated by Centurion Medical Products Corporation on October 23, 2017 and is designated Class II. Reason for recall: Convenience Kit containing components to assist practitioner with IV placement and securement. The recall status is terminated (terminated June 21, 2018). Affected quantity: N/A.
Recall Details
- Product Type
- Devices
- Report Date
- March 28, 2018
- Initiation Date
- October 23, 2017
- Termination Date
- June 21, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- N/A
Product Description
LATEX FREE IV START SET
Reason for Recall
Convenience Kit containing components to assist practitioner with IV placement and securement.
Distribution Pattern
Nationally
Code Information
IV4885 IV5600 Lot codes: 2015090790 2015112390 2016012590 2016030790 2016052390 2016062790 2016080890 2017010290 2017013090 2017031390 2017052290 2015110201 2016010401 2016040401 2016061301 2016071101 2016082201 2017021601 2017041790 2017052290 2016122701 2015092801 2016022201 2017031301 2017062690