Drug recall
Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921 - Product Usage: AXS Universal…
FDA recall event 87551 · Class II · Medela AG Medical Technology
Key facts
| Event ID | 87551 |
|---|---|
| Recall numbers | Z-1502-2021 |
| Recalling firm | Medela AG Medical Technology |
| Product type | Devices |
| Products | Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921 - Product Usage: AXS Universal Aspiration Tubing is used with the Dominant Flex Surgical Suction Pump. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect expiration date of "2023-07-24" on label of sterile tubing. Correct expiration date should be "2021-07-24". |
| Initiation date | Dec 2, 2020 |
| Report date | May 5, 2021 |
| Termination date | Jun 17, 2024 |
| City | Baai |
| Country | Switzerland |
| FEI number | 3002807523 |
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: