Z-0278-2009

S/P Orange 50g Glucose Tolerance Beverage, 10 oz glass bottles, 12 bottles/case, labeled in part ***Cardinal...

Name: Z-0278-2009 S/P Orange 50g Glucose Tolerance Beverage, 10 oz glass bottles, 12 bottles/case, labeled in part ***Cardinal...
Creator: Nerl Diagnostics LLC
Published: 2008-04-23
License: https://open.fda.gov/license/

NERL Diagnostics Corporation / initiated 2008-04-23 / Terminated

FDA source

Nerl Diagnostics LLC began a recall of S/P Orange 50g Glucose Tolerance Beverage, 10 oz glass bottles, 12 bottles/case, labeled in part ***Cardinal Health McGaw Park, IL 60085-6787 USA*** For... on 2008-04-23. The reason FDA records is "Beverage may contain glass particles". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0278-2009
Status: Terminated
Initiated: 2008-04-23
Posted: 2008-11-04
Terminated: 2012-11-26
Recalling firm: NERL Diagnostics Corporation
Product: S/P Orange 50g Glucose Tolerance Beverage, 10 oz glass bottles, 12 bottles/case, labeled in part ***Cardinal Health McGaw Park, IL 60085-6787 USA*** For prescription use only. Product is used in support of diagnostics testing for hyperglycemia and hypoglycemia.
Product code: MRV Drink, Glucose Tolerance
Reason for recall: Beverage may contain glass particles.
FDA root cause: Other
Action: The recalling firm notified distribution centers by letter dated 04/23/08 and advised of a single report of glass found in a bottle. The notifications further advised distributors to quarantine referenced product, notify their customers and return the enclosed reply form. Distributors were requested to return or destroy product for replacement. Please contact NERL Diagnostics, LLC at 1-401-824-2046 for assistance.
Quantity in commerce: 25908 bottles
Distribution: Nationwide.
Product codes and lots: lot 4067, Exp 12-2009

Product code MRV

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)