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U.S. Department of Health and Human Services

Class 3 Device Recall GranuFlo Dry Acid Concentrate

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 Class 3 Device Recall GranuFlo Dry Acid Concentratesee related information
Date Initiated by FirmNovember 26, 2012
Date PostedJanuary 17, 2013
Recall Status1 Terminated 3 on June 21, 2016
Recall NumberZ-0682-2013
Recall Event ID 63768
510(K)NumberK030497 
Product Classification Dialysate concentrate for hemodialysis (liquid or powder) - Product Code KPO
ProductFresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis 2.0K 2,5 Ca 0.75Mg .16.5GAL Catalog Number: OFD2223-3B Product Usage: GranuFlo is indicated in the treatment of acute and chronic renal failure during the hemodialysis treatment.
Code Information Lot Number:12NXGF012
Recalling Firm/
Manufacturer		 Fresenius Medical Care Holdings, Inc.
920 Winter St
Waltham MA 02451-1521
For Additional Information Contact
800-662-1237
Manufacturer Reason
for Recall		GranuFlo Dry Acid Concentrate may show discoloration
FDA Determined
Cause 2		Nonconforming Material/Component
ActionFresenius Medical Care North America notified consignees by telephone on November 26, 2012 and follow-up letter on November 30, 2012 of the product recall. On January 10, 2013, the firm expanded there recall to an additional 32 lots (34 lots total). Customers were instructed to examine their inventory immediately, discontinue use, place all units in quarantine and return to Fresenius Medical Care North America. Customers were advised to contact their Fresenius Medical Care Customer Service Team for instructions on how to return the recalled product. For questions contact the GranuFio Recall Line at 1-888-803-0509
Quantity in Commerce2493 units
DistributionUS Nationwide Distribution
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = KPO
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