Teleflex Medical Europe Ltd recalls Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551310 (b) 650704120

Recalled April 18, 2018 · FDA recall Z-1369-2018 · 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

4220 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

Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551310 (b) 650704120 551312 (c) 650704160 551316 Product Usage: RUSCH Simplastic Suprapubic Puncture Instruments are indicated for emergency suprapubic drainage of the bladder.

Manufacturer(s)

Teleflex Medical Europe Ltd

Made in

Ireland

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →