[Recalled] 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)
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | 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 |
|---|---|
| Brand / manufacturer | Teleflex Medical Europe Ltd |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1367-2018 |
| Country of notice | Ireland |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 15 March 2018 |
| EAN / barcode | 151174050 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in Ireland and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.