[Recalled] MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A — The connectors may not allow catheters to be inserted as intended if the connec… | FDA 2024-10-1
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A |
|---|---|
| Brand / manufacturer | MEDLINE INDUSTRIES, LP - Northfield |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0511-2025 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 16 October 2024 |
| EAN / barcode | 10193489888287 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
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 MEDLINE INDUSTRIES, LP - Northfield
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.