Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1367-2018 — 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) 21

U.S. FDA — Device Enforcement · Ireland · 2018-03-15 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1367-2018
Date of alert: 2018-03-15
Country / jurisdiction: Ireland
Risk level: Class II
Risk type: recall
Brand: Teleflex Medical Europe Ltd
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 151174050

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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