[Recalled] Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. PEDIATRIC CATH ANGIO PACK, Model Number: DYNJ54755B; b. PEDIATRIC MAX BARRIER KIT-LF, Model Number: DYNJ40306A;
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. PEDIATRIC CATH ANGIO PACK, Model Number: DYNJ54755B; b. PEDIATRIC MAX BARRIER KIT-LF, Model Number: DYNJ40306A; c. PERC PACK-LF, Model Number: DYNJ0774759P; d. PERCUTANEOUS VASCUL |
|---|---|
| Brand / manufacturer | MEDLINE INDUSTRIES, LP - Northfield |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2321-2023 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 15 May 2023 |
| EAN / barcode | 088994292536 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
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.