Drug recall
Omnisound Gel, 250 ml bottle and 5 L container; and EcoGel 200, 250 ml bottle; Manufactured by Eco-Med. For…
FDA recall event 88602 · Class I · Accelerated Care Plus Corporation
Key facts
| Event ID | 88602 |
|---|---|
| Recall numbers | Z-2518-2021 |
| Recalling firm | Accelerated Care Plus Corporation |
| Product type | Devices |
| Products | Omnisound Gel, 250 ml bottle and 5 L container; and EcoGel 200, 250 ml bottle; Manufactured by Eco-Med. For use in ultrasound procedures. |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address… |
| Initiation date | Aug 25, 2021 |
| Report date | Oct 6, 2021 |
| City | Reno |
| State | NV |
| Country | United States |
| FEI number | 1000119345 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: