FDA recall Z-0702-2020

Product

NATRELLE Resterilizable Sizers for the styles and sizes: Style 15, Style 20, Inspira X (responsive gel), Inspira F (responsive gel), Inspira LP (responsive gel), Inspira M (responsive gel), Inspira L (responsive gel), Inspira ST L (Soft Touch gel), Inspira ST LP (Soft Touch Gel), Inspira ST M (Soft Touch Gel), Inspira ST F (Soft Touch Gel), Inspira ST X (Soft Touch Gel) Style 10/UDI: NATRELLE Sty 10-360 Rstrl Sizer Gel Mod 10888628005587 NATRELLE Sty 10-390 Rstrl Sizer Gel Mod 10888628005594 NATRELLE Sty 10-420 Rstrl Sizer Gel Mod 10888628005600 NATRELLE Sty 10-450 Rstrl Sizer Gel Mod 10888628005617 NATRELLE Sty 10-480 Rstrl Sizer Gel Mod 10888628005624 NATRELLE Sty 10-510 Rstrl Sizer Gel Mod 10888628005631 NATRELLE Sty 10-700 Rstrl Sizer Gel Mod 10888628005679 NATRELLE Sty 10-750 Rstrl Sizer Gel Mod 10888628005686 NATRELLE Sty 10-800 Rstrl Sizer Gel Mod 10888628005693 Style 15/UDI: NATRELLE Sty 15-304 Rstrl Sizer Gel Mid 10888628005778 NATRELLE Sty 15-339 Rstrl Sizer

Reason for recall

The firm has became aware that 2D barcodes on breast implants and sizers may be unreadable by GS-1 configured scanners. These 2D barcodes contain a group separators between fixed-length element string in the UDI data chain of the 2D barcode, which is not formatted to the GS1 standard.

Distribution

US:AL, AR,AZ,CA,CO,DC,FL,GA,HI,IA,ID,IL,IN,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,ND,NE,NH,NJ,NM,NV,NY,OH,OK,OR,PA,PR,RI,SC,SD,TN,TX,UT,VA,WA,WI,WY

Key facts

Status

Terminated

Initiation date

2019-11-06

Report date

2019-12-25

Termination date

2021-07-09

Voluntary/Mandated

Voluntary: Firm initiated

Location

Irvine, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0702-2020