RecallDepth

4 ml FX Sodium Fluoride/Potassium Oxalate tube, Ref 454297 VACUETTE Glycolytic Inhibitor Tubes contain an antiglycolytic agent, sodium fluoride, and an anticoagulant, potassium oxalate. The product is suitable for the analysis of blood glucose and lactate

Company
Greiner Bio-One North America, Inc.
Recall Initiated
April 26, 2016
Terminated
August 22, 2016
Recall Number
Z-1923-2016
Quantity
250,800 pieces (209 cases)
Firm Location
Monroe, NC

Reason for Recall

The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low additive (sodium fluoride and potassium oxalate), which can effect analytical results for glucose and lactate.

Distribution

Nationwide Distribution to CA, FL, IL, KY, NY, PA, VA and Puerto Rico

Lot / Code Info

Lot A151137L

Root Cause

Process control

Action Taken

Greiner Bio-One North America, Inc. sent an Urgent Product Recall letter dated April 26, 2016, to all affected consignees. The letter requested that they stop distribution of the product and to provide Greiner with a list of their sub-accounts. The letter included a Product Disposition/Site Confirmation form which is to be returned to Greiner Bio-one. Consignees with questions were instructed to call 800-515-8112. For questions regarding this recall call 704-261-7823.

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