Teleflex Medical Europe Ltd recalls latex rebreathing bags due to missing allergy warning. Check product codes and batch numbers for affected items. Contact for remedy.
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.
Teleflex Medical Europe Ltd is recalling latex rebreathing bags because they lack a required allergy warning label. This could cause allergic reactions in sensitive individuals. Affected items have specific product codes and batch numbers listed in the recall.
These bags contain natural rubber latex which can cause allergic reactions in sensitive individuals. The product lacks a required warning label about this risk.
Healthcare professionals and patients using rebreathing bags for medical ventilation. Those with latex allergies are at higher risk.
Check for product codes (a) through (m) and corresponding batch numbers listed in the recall. The bags are used for medical ventilation.
Review the product codes and batch numbers listed in the recall to confirm if your item is affected.
The product lacks a required allergy warning label about natural rubber latex, which can cause allergic reactions in sensitive individuals.
Check the product codes and batch numbers listed in the recall to determine if your item is affected. If affected, contact Teleflex Medical Europe Ltd for further instructions.
The recall record does not specify a remedy.
We’ve drafted a message you can send Teleflex Medical Europe Ltd to request your refund or repair — edit it as you like.
Subject: Recall Z-1367-2018 — Teleflex Medical Europe Ltd Teleflex Medical Europe Ltd Hello, I own a Teleflex Medical Europe Ltd that is covered by recall Z-1367-2018 from Teleflex Medical Europe Ltd. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
