[Recalled] 4042LH: 3 mL Line Draw, Luer lock syringe (heparin concentration: 7 I.U. per mL)with Filter-Pro¿ device Arterial Blood Sampling Line Draw Syringes are sterile, single-use devices, in-vitro diagnostic devices used for the dr
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | 4042LH: 3 mL Line Draw, Luer lock syringe (heparin concentration: 7 I.U. per mL)with Filter-Pro¿ device Arterial Blood Sampling Line Draw Syringes are sterile, single-use devices, in-vitro diagnostic devices used for the drawing of arterial blood via an arterial line. The product is not for in |
|---|---|
| Brand / manufacturer | Smiths Medical ASD, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1185-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 22 November 2013 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw Syringes
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.