Gina & Yittle (GA)
Active Member
Just got this in my weekly FDA recall newsletter. There is an ongoing recall of certain lots of Lantus. I'm sure its been posted before but since they haven't found all of the lots yet, those of you using Lantus may want to check your boxes to make sure you're not part of the recall.
PRODUCT
Apidra� SoloStar� [insulin glulisine (rDNA origin) injection], 100 units/mL (U-100), packaged in boxes of five 3 mL prefilled pens, Rx only, NDC 0088-2502-05. Recall # D-017-2011
CODE
Lot # 0F151A; Exp 01/12
RECALLING FIRM/MANUFACTURER
Recalling Firm: Sanofi-Aventis, Bridgewater, NJ, by letters on September 28, 2010 and October 6, 2010.
Manufacturer: Sanofi Aventis Deutschland Gmb-H, Frankfurt am Main, Germany. Firm initiated recall is ongoing.
REASON
Lack of Assurance of Sterility.
VOLUME OF PRODUCT IN COMMERCE
22,044 boxes (5 pre-filled pens/box)
DISTRIBUTION
Nationwide
PRODUCT
Apidra� SoloStar� [insulin glulisine (rDNA origin) injection], 100 units/mL (U-100), packaged in boxes of five 3 mL prefilled pens, Rx only, NDC 0088-2502-05. Recall # D-017-2011
CODE
Lot # 0F151A; Exp 01/12
RECALLING FIRM/MANUFACTURER
Recalling Firm: Sanofi-Aventis, Bridgewater, NJ, by letters on September 28, 2010 and October 6, 2010.
Manufacturer: Sanofi Aventis Deutschland Gmb-H, Frankfurt am Main, Germany. Firm initiated recall is ongoing.
REASON
Lack of Assurance of Sterility.
VOLUME OF PRODUCT IN COMMERCE
22,044 boxes (5 pre-filled pens/box)
DISTRIBUTION
Nationwide