Teleflex Medical Europe Ltd: Medical Device Recall in 2018 - (Recall #: Z-1370-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 15, 2018

Date Posted: April 18, 2018

Recall Number: Z-1370-2018

Event ID: 79579

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.

Status: Terminated

Product Quantity: 200 units

Code Information:

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

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated