Z-1370-2018 Class II Terminated

Recalled by Teleflex Medical Europe Ltd — Athlone

Recall Details

Product Type
Devices
Report Date
April 18, 2018
Initiation Date
March 15, 2018
Termination Date
October 5, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
200 units

Product Description

Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b) 655500200 655520

Reason for Recall

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.

Distribution Pattern

US Nationwide Distribution

Code Information

(a) 655300160 655316 Batch Numbers 13EG28 13HG23 (b) 655500200 655520 Batch Numbers: 13EG28