Drug recall
Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory…
FDA recall event 75093 · Class II · ICU Medical, Inc.
Key facts
| Event ID | 75093 |
|---|---|
| Recall numbers | Z-0988-2017 |
| Recalling firm | ICU Medical, Inc. |
| Product type | Devices |
| Products | Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | ICU Medical Inc. has identified a potential risk of leaking with certain Tego Connector devices. |
| Initiation date | Aug 24, 2016 |
| Report date | Jan 18, 2017 |
| Termination date | Jul 7, 2017 |
| City | San Clemente |
| State | CA |
| Country | United States |
| FEI number | 2025816 |
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: