ConvaTec Flexi-Seal Fecal Management System Advanced Odor Control Kit. Rx only; 1 silicone catheter tube assembly, 3-1 Liter collection bags with filters, 1 luer-lock syringe, SKU #411104 ConvaTec Skillman, NJ Made in USA with imported components "For the fecal management of patients with little or no bowel control and liquid or semi-liquid stool." Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Flexi-Seal Fecal Management System Advanced Odor Control Kit. Rx only; 1 silicone catheter tube assembly, 3-1 Liter collection bags with filters, 1 luer-lock syringe, SKU #411104 ConvaTec Skillman, NJ Made in USA with imported components "For the fecal management of patients with little or no bowel control and liquid or semi-liquid stool."
Brand
ConvaTec
Lot Codes / Batch Numbers
Lot number 08-TM-51
Products Sold
Lot number 08-TM-51
ConvaTec is recalling Flexi-Seal Fecal Management System Advanced Odor Control Kit. Rx only; 1 silicone catheter tube asse due to It was discovered that a portion of the inner nylon sleeve of the catheter was visible at the balloon end of a sample device.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
It was discovered that a portion of the inner nylon sleeve of the catheter was visible at the balloon end of a sample device.
Recommended Action
Per FDA guidance
Urgent Product Correction Letters were sent by first class mail on November 18, 2008 to Healthcare Professionals and ConvaTec Reps. The reason for the recall was identified along with possible risk to patient. Healthcare professionals were asked to use sufficient lubricating jelly during the insertion process with special care given to those who have a tendency to bleed or are on anti-coagulant medication. Physician should be notified if rectal bleeding or abdominal symptoms develop. ConvaTec reps were asked to contact all health care professionals to whom product or samples were given and reinforce the importance of proper lubrication and following the directions. A return form is to be completed by ConvaTec reps for each visit indicating the name of the Health Care Provider and that the they personally received notice of the product correction. All remaining sample products are to be returned to Besta, Franklin, WI.
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 noticePage updated: Jan 10, 2026