FDA Device recall Z-2619-2023
MINISCAV (tm) Vacuum Pump
- FDA Device
- Class II
- ongoing
- Published 2023-09-27
On 2023-09-27 the FDA classified a Class II recall of MINISCAV (tm) Vacuum Pump by R A Medical Services, citing inadequate documentation of acceptance activity.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2619-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-08-23 |
| Published | 2023-09-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | R A Medical Services |
| Distribution | OH |
Product
MINISCAV (tm) Vacuum Pump
Reason
Inadequate documentation of acceptance activity
Identifiers
| code_info | UDI/DI: (01) 10862552000405. Serial numbers: N/AB/10514 through N/AB/10523 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2619-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.