Abbott Laboratories HPD/ADD/GPRD Pentalumen TD Thermodilution Catheter, Sterile Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pentalumen TD Thermodilution Catheter, Sterile
Brand
Abbott Laboratories HPD/ADD/GPRD
Lot Codes / Batch Numbers
List No. 41233-01, Lot 04-187-SN
Products Sold
List No. 41233-01, Lot 04-187-SN
Abbott Laboratories HPD/ADD/GPRD is recalling Pentalumen TD Thermodilution Catheter, Sterile due to Thermodilution catheters have a potential for ruptured lumens within the catheter.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Thermodilution catheters have a potential for ruptured lumens within the catheter.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 11/19/2003.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, AR, CA, FL, IN, LA, MA, NC, OR, PA, TN, TX, UT, VA, WA
Page updated: Jan 10, 2026