FDA recall D-0934-2017

Product

Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Pump in 0.9% Sodium Chloride Injection, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-100-13

Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date

Distribution

Nationwide

Key facts

Status

Terminated

Initiation date

2017-02-15

Report date

2017-07-12

Termination date

2020-01-13

Voluntary/Mandated

Voluntary: Firm initiated

Location

Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0934-2017