May 24, 2012

Moog Medical Devices Group Recalls Select Curlin Administration Sets

The Missouri Department of Health and Senior Services received the following news release regarding the recall of certain lots of Curlin Intravenous Administration Sets.

Use of the affected sets may cause desanguination (blood loss), an under-delivery of prescribed medication/fluid, or a potential delay in therapy. Continued use of the affected administration sets may cause a potential risk of serious injury or death.

The following REF (catalog) and lot numbers, which were sold and distributed in the U.S. between December 2011 and May 2012, are included in the recall:

REF Code (REF Codes are found in the top right hand corner of the administration set packaging):

340-4114

340-4115

340-4126

340-4128

340-4128-V

340-4130

340-4130-V

340-4133

340-4137

340-4144

340-4165

340-4166

340-4173

340-4176

Lot Numbers (Lot numbers are found in the lower right hand corner of the administration set packaging):

CF1127990

CF1134390

CF1200492

CF1202592

CF1205492

CF1208091

CF1127991

CF1134391

CF1200493

CF1204092

CF1206890

CF1208092

CF1127992

CF1133490

CF1200293

CF1204093

CF1206891

CF1129990

CF1134392

CF1200494

CF1203391

CF1205493

CF1130190

CF1134990

CF1200294

CF1204091

CF1206090

CF1130690

CF1134393

CF1201893

CF1203392

CF1206091

CF1130691

CF1135490

CF1201890

CF1203390

CF1206092

CF1130693

CF1135491

CF1201190

CF1204090

CF1208090

CF1131190

CF1135492

CF1201192

CF1204690

CF1206893

CF1131191

CF1200290

CF1202591

CF1204691

CF1207592

CF1130692

CF1200291

CF1202590

CF1205491

CF1207590

CF1132290

CF1200292

CF1201891

CF1204692

CF1207591

CF1132291

CF1200490

CF1201191

CF1205490

CF1207593

CF1133491

CF1200491

CF1201892

CF1205990

CF1209091

The full recall can be found at www.fda.gov/Safety/Recalls/ucm305208.htm?source=govdelivery.


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