Drug recall
Stryker SmartLife Large Aseptic Housing (7126-120-000)
FDA recall event 76739 · Class II · Stryker Instruments Div. of Stryker Corporation
Key facts
| Event ID | 76739 |
|---|---|
| Recall numbers | Z-1886-2017 |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation |
| Product type | Devices |
| Products | Stryker SmartLife Large Aseptic Housing (7126-120-000) |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Stryker Instruments issued a notice of correction for an update to cleaning practices for the Stryker SmartLife Large Aseptic Housings following complaints of deterioration to the housing and the top… |
| Initiation date | Feb 28, 2017 |
| Report date | May 3, 2017 |
| Termination date | Jan 23, 2023 |
| City | Portage |
| State | MI |
| Country | United States |
| FEI number | 1811755 |
At a glance
- 1–9 Products in this recall
- 10–99 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: