Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 Recalled by Teleflex Medical Europe Ltd Due to These products contain latex, but the following statement...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teleflex Medical Europe Ltd directly.
Affected Products
Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 (b) 153000005 153000005 (c) 153000010 153000010 (d) 153000020 153000020 (e) 153000030 153000030 (f) 153000050 153000050 (g) 210700050 2107050 (h) 210700102 2107102 (I) 210700202 2107202 (j) 210700302 2107302 (k) 210700402 2107402 (l) 210700502 2107502 (m) 210700602 2107602 Product Usage: Rebreathing Bag is indicated for manual patient ventilation or in connection with anaesthesia apparatus and/or patient ventilators.
Quantity: 107962 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teleflex Medical Europe Ltd
Teleflex Medical Europe Ltd has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report