Z-1946-2020 Class II Terminated
FDA device recall Z-1946-2020 was initiated by Becton Dickinson & Company on March 17, 2020 and is designated Class II. Reason for recall: Iincorrectly packaged without the required lidocaine as labeled The recall status is terminated (terminated October 21, 2020). Affected quantity: 655 kits.
Recall Details
- Product Type
- Devices
- Report Date
- May 20, 2020
- Initiation Date
- March 17, 2020
- Termination Date
- October 21, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 655 kits
Product Description
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Reason for Recall
Iincorrectly packaged without the required lidocaine as labeled
Distribution Pattern
AZ, CT, GA, IL, LA, MA, MI, MN, ND, NE, NY, OH, SD, TX),
Code Information
Lot Number: REDW0476 20 Exp. Date: 20OCT30 UDI: (01)00801741139390