FDA Drug Recalls

Recalls / Class III

Class IIID-0907-2017

Product

Potassium CHLORide added to 0.9% Sodium Chloride, 10mEq 100 mL Bag, Service Code 2K5856, NDC# 61553-0856-48, Total Volume 100.00 mL incorrectly labeled as 105.00 mL, Rx Only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 38141

Affected lot / code info
Lot Numbers: 163640167M, 3/21/2017; 170050171M, 3/28/2017; 170070172M, 3/31/2017;170190235M, 4/11/2017; 170200120M, 4/14/2017; 170230115M, 4/15/2017; 170390059D, 5/10/2017;

Why it was recalled

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Recalling firm

Firm
Pharmedium Services, LLC
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
150 N Field Dr Ste 350, N/A, Lake Forest, Illinois 60045-2506

Distribution

Quantity
143 bags
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2017-02-17
FDA classified
2017-06-12
Posted by FDA
2017-06-21
Terminated
2017-06-13
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0907-2017. 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