Drug recall
SunTech Medical Disposable, Neonate #4, 1-Tube, Male Bayonet, Blood Pressure Cuffs, Box of 20
FDA recall event 83070 · Class II · Suntech Medical, Inc.
Key facts
| Event ID | 83070 |
|---|---|
| Recall numbers | Z-2277-2019 |
| Recalling firm | Suntech Medical, Inc. |
| Product type | Devices |
| Products | SunTech Medical Disposable, Neonate #4, 1-Tube, Male Bayonet, Blood Pressure Cuffs, Box of 20 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product is mislabeled. The label on the package is for a size #4 cuff, but the incorrect size #3 cuff was placed in the package. |
| Initiation date | Jun 3, 2019 |
| Report date | Aug 21, 2019 |
| Termination date | Dec 16, 2020 |
| City | Morrisville |
| State | NC |
| Country | United States |
| FEI number | 1036863 |
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: