FDA Drug Recalls

Recalls / Class III

Class IIID-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

Affected lot / code info
Lot: 170310113s; Exp. 01/01/1900

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date

Recalling firm

Firm
Pharmedium Services Llc
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
150 N Field Dr, N/A, Lake Forest, Illinois 60045-4847

Distribution

Quantity
21 I.V. pumps
Distribution pattern
Nationwide

Timeline

Recall initiated
2017-02-15
FDA classified
2017-07-02
Posted by FDA
2017-07-12
Terminated
2020-01-13
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0934-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class III recall: drug · FDA Drug Recalls