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Teleflex Medical Europe Ltd recalls Rectal Catheters; Product Code Equivalent Code 580114 580114 Product Usage: Rectal Balloon Catheter i
Recalled April 18, 2018 · FDA recall Z-1368-2018 · Teleflex Medical Europe
Hazard
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions. · FDA Class II
Units
6340 units
Sold at
US Nationwide Distribution
Description
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
Product
Rectal Catheters; Product Code Equivalent Code 580114 580114 Product Usage: Rectal Balloon Catheter is inserted into the rectum to measure the abdominal pressure as bladder filled.
Manufacturer(s)
Teleflex Medical Europe Ltd
Made in
Ireland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →