[Recalled] Smiths Medical CADD Blue-Striped IV Administration Set, REF 21-7036-01, Sterilized using ethylene oxide. — The label of the CADD Blue-Striped Administrative Set is missing the expiration… | FDA 2016-12-09
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Smiths Medical CADD Blue-Striped IV Administration Set, REF 21-7036-01, Sterilized using ethylene oxide. |
|---|---|
| Brand / manufacturer | Smiths Medical ASD Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2759-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 09 December 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The label of the CADD Blue-Striped Administrative Set is missing the expiration date, which is considered a regulatory compliance issue for Canada.
This Class II recall concerns device products distributed in United States 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 →
Related recalls from Smiths Medical ASD Inc.
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.