[Recalled] Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body. They are intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatmen
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body. They are intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatment or prevention of disease, or to affect the structure or any function |
|---|---|
| Brand / manufacturer | International Medsurg Connection, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2804-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 23 June 2017 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Insufficient documentation to support product sterility claims.
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 International Medsurg Connection, 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.