Z-2077-2020 Class II Terminated

Recalled by Becton Dickinson & Company — Franklin Lakes, NJ

FDA device recall Z-2077-2020 was initiated by Becton Dickinson & Company on February 26, 2020 and is designated Class II. Reason for recall: The kits contain surgical gowns which were subject to a recall by the supplier. The recall status is terminated (terminated September 22, 2020). Affected quantity: 1262 total.

Recall Details

Product Type
Devices
Report Date
May 27, 2020
Initiation Date
February 26, 2020
Termination Date
September 22, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1262 total

Product Description

BARD MYPICC KIT 4F Single-Lumen, Catalog Number CK000276

Reason for Recall

The kits contain surgical gowns which were subject to a recall by the supplier.

Distribution Pattern

The products were distributed to the following US states: IN, MO, OH, and TX.

Code Information

Lot Numbers: 18JBB605 18KBZ117 19EBE196 19GBG860 19SBH077 19UBA090