FDA recall Z-0263-2020

Product

Autoject EI, REF AJ1310

Reason for recall

There is a possible assembly error on Autoject EI, lot number V14. This lot was packed into two products: AJ 1310, lot number V14 and AN 3310VET (branded as Petfine Auto Injector), batches V14.V976 & V14.W107

Distribution

FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA

Key facts

Status

Ongoing

Initiation date

2019-07-17

Report date

2019-11-13

Voluntary/Mandated

Voluntary: Firm initiated

Location

Marietta, GA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0263-2020